Hypodermic syringe needle assembly and method of making the same Number:7,393,344 from the United States Patent and Trademark Office (PTO) owispatent A retractable needle assembly for use in medical procedures comprising a needle assembly including a hub, a hollow needle passing through the hub and projecting from the posterior end of the hub. A tubular sheath having a longitudinal slot extending along a portion of its length A post attached to the hub and positioned to project through said longitudinal slot such that the needle and hub assembly may slide along the length of the sheath from a position exposing said needle to a retracted position within said sheath. A means for reversibly locking the needle assembly in the retracted position, a means for reversibly locking the needle in the in the exposed position and means for permanently locking the needle in the retracted position. Several different embodiments for locking the needle assembly in position both reversibly or permanently are disclosed.<H Hypodermic, assembly, Hypodermic, syri, 7393344.html, Patent, pto, 7393344

Title: Hypodermic syringe needle assembly and method of making the same

Abstract: A retractable needle assembly for use in medical procedures comprising a needle assembly including a hub, a hollow needle passing through the hub and projecting from the posterior end of the hub. A tubular sheath having a longitudinal slot extending along a portion of its length A post attached to the hub and positioned to project through said longitudinal slot such that the needle and hub assembly may slide along the length of the sheath from a position exposing said needle to a retracted position within said sheath. A means for reversibly locking the needle assembly in the retracted position, a means for reversibly locking the needle in the in the exposed position and means for permanently locking the needle in the retracted position. Several different embodiments for locking the needle assembly in position both reversibly or permanently are disclosed.

Patent Number: 7,393,344 Issued on 07/01/2008 to Mohammed

Inventors: Mohammed; Owais (Riverdale, MD)
Appl. No.: 10/670,362

Filed: September 26, 2003

Related U.S. Patent Documents


Application Number	Filing Date	Patent Number	Issue Date
10157885	May., 2002	6926696
10133491	Apr., 2002	6776775
09613753	Jul., 2000	6669671
09471094	Dec., 1999	6379337

Current U.S. Class: 604/195 ; 604/198; 604/272

Current International Class: A61M 5/32 (20060101)

Field of Search: 604/162,163,164.08,168.01,187,192,195,197,198,240,263,264,272,403,411,414,415,900 60/573,576,577 606/167,185,187

References Cited [Referenced By]

U.S. Patent Documents


6926696	August 2005	Mohammed

Primary Examiner: Mendez; Manuel
Attorney, Agent or Firm: Bacon & Thomas, PLLC

Parent Case Text

REFERENCE TO RELATED APPLICATION

This application is a continuation-in-part of Ser. No. 10/157,885, filed May 31, 2002 now U.S. Pat. No. 6,926,696, which is a continuation-in-part of Ser. No. 10/133,491, filed on Apr. 29, 2002 now U.S. Pat. No. 6,776,775, which is a continuation-in-part of Ser. No. 09/613,753, filed Jul. 11, 2000 now U.S. Pat. No. 6,669,671, which is a continuation-in-part of Ser. No. 09/471,094, filed Dec. 23, 1999 now U.S. Pat. No. 6,379,337. The disclosure of the applications cited above is incorporated by reference herein. Additionally, the disclosure of each of the following applications having Owais Mohammed named as inventor is incorporated by reference herein: Ser. No. 09/218,040, filed Dec. 22, 1998; and Ser. No. 09/316,047, filed May 21, 1999.

Claims

What is claimed is:

1. A retractable needle assembly for use in medical procedures, comprising: a needle assembly, said needle assembly comprising a hub having an anterior end and a posterior end, a hollow needle attached to the posterior end of the hub; a tubular sheath having a longitudinal slot along a portion of its length, an anterior end, and a posterior end, said posterior end having an opening therethrough, wherein the needle assembly is positioned within the tubular sheath with the hollow needle projecting from the posterior end of the hub through the posterior end of said sheath; a cap attached to the anterior end of said sheath, said cap being open at its anterior end to allow access to the interior of said sheath; a post, attached to said hub and projecting through said longitudinal slot; a cross piece attached to the top of said post for moving the needle assembly along said longitudinal slot; wherein said needle assembly may be moved reversibly along said longitudinal slot of said sheath between an exposed position in which the hollow needle passes through the opening in the posterior end of the sheath and a retracted position in which the hollow needle is contained within the tubular sheath, wherein the opening in the posterior end of the sheath is large enough to allow the hollow needle to pass therethrough, but too small to allow the hub to pass therethrough; a means for reversibly locking the needle assembly in its exposed position; a means for reversibly locking the needle assembly in its retracted position; means for permanently locking the needle assembly in its retracted position, said permanent locking means comprising an aperture in said cap and a pin extending radially from said post which is received into said aperture.

2. The retractable needle assembly according to claim 1 wherein said pin includes a tapered surface forming a ramp, which engages said cap and "squeezes" said pin when said post is being inserted into said cap.

3. The retractable needle assembly according to claim 1 wherein said cap includes at least one lateral wall which partly defines a space which includes said aperture.

4. The retractable assembly according to claim 1 wherein said cap includes one lateral wall and a partial one of another lateral wall.

Description

BACKGROUND OF THE INVENTION

The present invention generally refers to hypodermic syringe needles for medical use. More particularly, the invention relates to hypodermic safety needles which retract into a container when not in use, preventing unintentional contact with the needle.

Prior art injection needles feature hollow needles which extend through a plastic hub. To prevent a user from accidentally pricking himself with the point of a needle, the needle is covered with a removable cover. Such covers frictionally engage the plastic hub, and may be readily removed once the needle is attached to a syringe barrel. After use, the cover may be reattached to the needle assembly, which is then separated from the syringe barrel and discarded. However, there is an unacceptable risk of accidental injury resulting from contact with the point of the needle during the recapping step. This is particularly dangerous as biological fluids contaminating the needle could enter the user's bloodstream. An improved means of covering a used injection needle is needed.

A wide variety of needles having a means for shielding a syringe needle from accidental contact with a user's fingers have been developed. For example, U.S. Pat. No. 4,900,311, "Hypodermic Syringe", issued to Stern on Feb. 13, 1990, relates to a hypodermic syringe having a syringe barrel, an injection needle attached to the syringe barrel, and a needle guard of elliptical cross section disposed around the syringe barrel. The needle guard may be moved from a first position which covers the needle to a second position which exposes the needle. When the guard is in the second position, tabs on the interior of the guard engage slots on the syringe barrel, locking the guard into position. When the tabs are released from the slots by squeezing the elliptical guard along its longitudinal axis, a spring causes the guard to move into the first position, hiding the needle. The entire syringe assembly is then discarded.

This device, while useful, does have certain drawbacks. The syringe barrel used with this assembly has a highly specialized structure; a generic syringe barrel cannot readily be substituted. Also, the syringe barrel cannot readily be sterilized and reused. No provision for separation of the needle from the syringe barrel without removing the syringe needle from the protective needle guard is provided. Finally, there is the risk of accidentally squeezing the elliptical needle guard, causing the spring to move the needle guard into a position which conceals the needle prior to use of the needle.

U.S. Pat. No. 4,664,654, "Automatic protracting and locking hypodermic needle guard", issued to Strauss on May 12, 1987, relates to a two-piece needle shield comprising a sliding member and a stationary member. A latch holds the sliding member in position. When the latch is released, a spring causes the sliding member to retract inside the stationary member, exposing the needle. However, this device causes the user to place his hand in proximity to the needle at the time it is exposed, increasing the likelihood of injury from accidental contact with the needle.

U.S. Pat. No. 5,246,428, "Needle Safety Mechanism", issued to Falknor on Sept. 21, 1993, relates to a needle safety mechanism comprising a base adapted to be fixed with respect to the needle, and a sheath which is movable between a first position which exposes the needle and a second position which covers the needle. A latch cooperative between the base and the sheath may be used to releasably latch the sheath in the position which covers the needle. A spring biases the sheath into the needle covering position. No mechanism for latching the sheath in a position which exposes the needle is provided, however. This may be an inconvenience for workers who wish to see the precise spot where they are administering an injection.

U.S. Pat. No. 5,279,579, "Self-recapping Injection Needle Assembly", issued to D'Amico on Jan. 18, 1994, relates to a self-capping injection needle assembly which includes a hub slidably positioned within a cylindrical cover adapted to receive a syringe barrel, and a needle mounted on the hub. A spring biases the hub into a position in which the needle is contained within the tubular cover. When the spring is compressed, the hub may slide into a position which exposes the needle. The hub includes a pin which slidably engages a longitudinal groove in the tubular cover. The groove includes a transverse leg adapted to receive the pin. When the pin is positioned in the transverse leg, the hub is releasably locked into a position which exposes the needle. The hub has a threaded female joint which may be screwed onto a syringe barrel having a corresponded threaded male joint. Different size tubular covers may be used for different size syringe barrels.

This device has certain disadvantages. First, in a medical environment time is often a critical factor. A more rapid method of affixing a needle to a syringe barrel than screwing it on is desirable. Also, only syringe barrels with a specific type of joint adapted to mate with the hub are usable with this device. Most commonly used medical syringe barrels have frusto-conical tips which frictionally engage syringe needle hubs having frusto-conical cavities therein; such commonly used barrels cannot be used with the threaded connections envisioned by D'Amico. D'Amico requires that a hub having a specific diameter must be used with a tubular cover having an inner diameter which is substantially equal to the hub diameter. Most commonly available syringe needle hubs have a single standard size, and cannot be used with a range of tubular cover sizes. Therefore, D'Amico's invention necessitates creation of a range of expensive and specialized syringe needles having a range of hub sizes. Also, since the diameter of D'Amico's hub is very nearly equal to the interior diameter of the tubular cover, it is difficult to insert a hub having a protruding pin into the cover. An easy method of assembling such a device is desirable.

There is a long-felt need in the art for a safety needle assembly having a retractable needle which may be easily assembled, and which may be used with commonly available syringe barrels having frusto-conical tips which frictionally engage a syringe needle assembly. The required safety needle assembly must also avoid the other disadvantages of known prior art devices. It is an object of this invention to provide such a safety needle assembly.

SUMMARY OF THE INVENTION

The present invention provides a disposable hypodermic syringe needle which retracts into a container for safe disposal. The retractable needle assembly comprises: a needle assembly, said needle assembly comprising a hub having an anterior end and a posterior end, a hollow needle passing through the hub and projecting from the posterior end of the hub; and a tubular sleeve connected with a peripheral edge of the hub and projecting from the anterior end of the hub, said sleeve having a radially directed hole therethrough; and a tubular sheath having a wall with a radially directed hole therethrough, an anterior end, and a posterior end, said posterior end having an opening therethrough. The needle assembly is positioned within the tubular sheath with the hollow needle being directed toward the opening in the posterior end of the sheath. The needle assembly may be moved reversibly along the axis of the sheath between an exposed position in which the hollow needle passes through the opening in the posterior end of the sheath and a retracted position in which the hollow needle is contained within the tubular sheath. The retractable needle assembly further comprises a plurality of locking mechanisms, each designed to lock the needle assembly into a specified position. The needle assembly comprises a means for reversibly locking the needle assembly in its exposed position; a means for reversibly locking the needle assembly in its retracted position; and a means for permanently locking the needle assembly in its retracted position. In one embodiment, the permanent locking means comprises a radially-directed peg mounted on an exterior surface of the tubular sheath so that one end of the radially-directed peg is adapted to be pushed inwardly through the hole in the wall of the tubular sheath and through the hole in the tubular sleeve. This end of the radially-directed peg may not be withdrawn through the hole in the tubular sleeve after it has been pushed through the hole in the tubular sleeve. Other embodiments of the permanent locking means are also feasible.

Preferably, the tubular sheath or container features a tubular wall having a longitudinal slot therethrough. One end of the container is open so that a syringe barrel may be received therein. The second, or posterior, end of the container has an opening which is sufficiently large to allow a hypodermic needle to pass therethrough, but is too small to allow the hub or a syringe barrel to pass therethrough. A spring may engage the hub of the needle assembly and a ridge on the interior of the wall of the second end of the container. This spring biases the hub away from the second end of the container so that the needle attached to the hub is hidden within the container. When the spring is compressed, the needle is able to pass through the opening of the posterior end of the container. A pin attached to the annular sleeve is slidably engaged by the longitudinal slot in the container wall, holding the needle within the container while allowing it to slide back and forth. A knob mounted on the pin is positioned outside the container. The knob is too large to pass through the longitudinal slot, and acts to position the hub of the needle along the axis of the container. When the knob is pushed toward the second end of the container, the hub moves toward the second end of the container, compressing the spring and causing the needle to emerge through the second open end of the container. A means for reversibly engaging the knob when the spring is compressed is also provided. This allows the needle to be retained in an exposed position.

The needle may be frictionally secured to a syringe barrel having a plunger slidably mounted therein. More specifically, a syringe barrel having a tip is secured to the needle assembly by inserting the tip of the syringe barrel into the cavity of the annular sleeve until the barrel tip is frictionally secured to the barrel sleeve. Additional features of the invention will be described in the detailed description of the preferred embodiments. Any syringe barrel having an appropriately shaped tip may be used with the inventive needle assembly.

Other embodiments of this invention are contemplated. The needle assembly of invention may be attached to an IV tube and used for intravenous administration of ids. Also, a modified needle assembly having a double-ended hypodermic needle that is fixed to a hub may be used to withdraw samples of venous blood.

DESCRIPTION OF THE DRAWINGS

FIG. 1a illustrates a side view of a preferred needle assembly for use in the syringe assembly of this invention.

FIG. 1b, 1c, and 1d illustrate cross-sectional views of preferred needle assembly.

FIG. 1e illustrates an end view of the needle assembly of FIG. 1a.

FIGS. 2 and 3 show grooved containers designed to contain the needle of FIG. 1a.

FIG. 4 shows a retractable hypodermic safety needle within a container, with the needle in a retracted configuration.

FIG. 5 shows a retractable hypodermic safety needle within a container, with the needle in an exposed configuration.

FIGS. 6a through 6g show various embodiments of locking mechanisms to hold a retractable needle in an exposed configuration.

FIGS. 7, 8a, 8b, 8c, 9a, 9b, 9c, 9d, 9e, 9f, 10a, 10b, 10c and 10d show mechanisms to irreversibly lock a retractable needle in a retracted configuration.

FIG. 11 is an exploded view of the syringe of the current invention, showing how the pieces are assembled.

FIG. 12 illustrates the parts used to form an alternate version of the container of FIG. 2.

FIG. 13 is an exploded view of the retractable hypodermic safety needle within a container shown in FIG. 12.

FIGS. 14 and 15 show a modified version of the apparatus of FIG. 4.

FIGS. 16 and 17 show a second modified version of the apparatus of FIG. 4.

FIG. 18 shows a modified version of the needle assembly of FIG. 1a, for use in taking blood samples.

FIG. 19 shows an apparatus for taking blood samples, using the needle assembly of FIG. 18.

FIG. 20 shows how rigid ring 9a fits onto the tubular container of FIG. 2.

FIG. 21 shows the apparatus of FIG. 19 in use.

FIG. 22, 22a, 23a, 23b, 23c, 25c, and 25d show a needle assembly featuring an adjustable-length tube.

FIGS. 24a, 24b, 25a, and 25b show different embodiments of the adjustable-length tube.

FIG. 26 shows the apparatus of FIG. 22 in use.

FIG. 27 shows a needle assembly for use with a catheter.

FIG. 28 shows a retractable needle for use with a catheter.

FIG. 29 shows a preferred housing design for use with a catheter.

FIG. 30 shows the needle assembly of FIG. 28 with a catheter attached thereto.

FIGS. 31a through 31d show a catheter adapted for use with the catheter assembly of claim 27, said catheter having a stopcock assembly.

FIGS. 32a, and 32b show means for reversible locking a needle assembly in the retracted and exposed positions.

FIG. 32c shows a means for reversibly locking a needle assembly in the exposed position using a tapered slot.

FIG. 32d shows a tapered sheath with a tapered slot.

FIG. 33a shows a sectional view of permanent needle locking means in the open position. FIG. 33d shows a blind hemispherical hole in the cross piece of FIG. 33a.

FIG. 34a shows a sectional view of another one of the permanent locking mechanisms in the unlocked position.

FIG. 33b shows the embodiment of FIG. 34a in the locked position.

FIG. 33c is a plan view of the device of FIG. 33a.

FIG. 34b shows the embodiment of FIG. 34a in the locked position.

FIG. 34c is a plan view of the device of FIG. 34a.

FIG. 34d is an elevation view of the guard of FIGS. 33 and 34.

FIG. 34e is an alternate embodiment of the device of FIG. 34a.

FIG. 35a is a partial sectional view of an alternate embodiment of the invention.

FIG. 35b is a plan view of FIG. 35a showing the reversible tapered locking slot.

FIG. 35c is a rotated plan view of the device of FIGS. 35a.

FIG. 35d a sectional view of the tubular connector of FIG. 35.

FIG. 35e is a sectional of another tubular connector of FIG. 35.

FIG. 35f is an alternate locking means for the device of FIG. 35a.

FIG. 36a is a partial sectional view of another embodiment of the invention.

FIG. 36b is a plan view of the device of FIG. 35a having a tapered slot.

FIG. 36c is a partial plan view of FIG. 36a showing an alternate locking means.

FIG. 37 is a partial sectional view of an alternate embodiment of the invention.

FIG. 37a is an alternate embodiment of the invention of FIG. 37.

FIG. 37b is another embodiment of the invention of FIG. 37a.

FIG. 38 is an alternate embodiment of the invention of FIGS. 33a-33d.

DETAILED DESCRIPTION

The needle used in the present invention is designed for use with a syringe comprising a plunger and a syringe barrel having a tubular wall with a defined outer diameter, where the barrel has an open end adapted to receive the plunger and a closed end having a cylindrically symmetric tip projecting therefrom. The tip of the barrel has a defined diameter which is less than the defined outer diameter of the syringe barrel and a longitudinal bore passing through the tip and the closed end of the barrel.

FIG. 1a illustrates a hypodermic needle for use in the syringe assembly of this invention. Needle 1 is affixed to hub 2. A hollow bore runs longitudinally through needle 1 and hub 2. An annular sleeve 3 is affixed to the outer periphery 4 of hub 2. A ledge 5 encircling hub 2 is defined by the edge of sleeve 3. Sleeve 3 defines a cavity 6 adapted to frictionally engage the tip of the syringe barrel, as shown in the cross-sectional views of FIGS. 1b and 1c. The diameter of cavity 6 is sized to match the diameter of the tip of the syringe barrel, while being substantially smaller than the diameter of the outer diameter of the tubular wall of the syringe barrel, allowing the cavity 6 to fit over the syringe barrel tip without extending over the external surface of the wall of the syringe barrel. In one preferred embodiment, the interior surface of the sleeve defines a frusto-conical cavity 6, where the sleeve is adapted to frictionally engage a frusto-conical tip of a syringe barrel (FIG. 1b). In another preferred embodiment, the interior surface of the sleeve defines a cylindrical cavity of constant diameter, where the sleeve is adapted to frictionally engage a cylindrical syringe barrel tip of constant diameter (FIG. 1c). Alternatively, the interior surface of the tubular sleeve may be threaded, allowing it to engage a threaded male joint on the syringe barrel. If desired, the exterior surface of the tubular sleeve may be threaded, allowing it to engage a threaded female joint on the syringe barrel. Finally, the user may wish to connect the needle to a syringe barrel having a Luer-Loc.RTM. connector. Such a connector typically includes a threaded female joint on the syringe barrel, surrounding a non-threaded male joint on the syringe barrel. The interior surface of the tubular sleeve frictionally engages the inner male joint on the Luer-Loc.RTM. connector on the syringe barrel, while a flange 3a on the exterior surface of the tubular sleeve engages the threaded female joint on the syringe barrel, as shown in FIG. 1d.

A radially projecting member 7 is affixed to the outer surface of sleeve 3. A thumb rest knob or crosspiece 8 is mounted on member 7. Member 7 commonly takes the form of a pin having a round cross section; however, other configurations are possible. Member 7 may have a square, rectangular, or oval cross section. If desired, 7 may have a length which is substantially greater than its width. The crosspiece may take any of several forms. It may be square. It may also be a round disk, a spherical knob, or a hemispherical knob. It may also take the form of a ring which encircles hub 2, without being connected to hub 2, except by means of stem 7. Crosspiece 8 should be positioned so that, when viewed along the axis of needle 1, piece 8 and pin 7 intersect at a right angle (FIG. 1e). Although pin 7 and crosspiece 8 may be manufactured separately and secured together, it is preferred that 7 and 8 be manufactured as a single piece.

FIG. 2 shows a grooved container designed to house the needle of FIG. 1a. The container has a tubular wall 9 having a longitudinal slot 10 therethrough. A first end of the container has an opening 13 adapted to receive a syringe barrel. The second end of the container has an opening 14 which is large enough to allow needle 1 to pass therethrough, but too small to admit a syringe barrel or a human finger. A ledge 15 on the second end of the container runs from the interior of wall 9 to the edge of opening 14. Slot 10 runs from a point near the first end of the container, without reaching the first end of the container, to a point near the second end of the container, without reaching the second end of the container. A second slot 10a, running a part of the way around the circumference of wall 9, intersects slot 10 near the second end of the container. A similar slot 10b intersects slot 10 near the first end of the container. Slots 10a and 10b are preferably parallel to each other. A series of circumferential ridges 120 may optionally be positioned on the exterior of the container, said ridges being effective to strengthen the container, although this feature is not necessary for proper function of the invention. Slots 10a and 10b are preferably L-shaped slots, as shown in FIG. 2, or straight slots, as shown in FIG. 3. The slots 10a and 10b may have one or more teeth 200.

Although the container may be made in a single piece, it is preferred to manufacture the container in two pieces (FIG. 3). The first piece is a housing or a container having a tubular wall 9 with a longitudinal slot 10 therethrough, exactly as previously described; the sole difference is that the longitudinal slot 10 extends from the first open end of the container to a defined point near the second open end of the container, slot 10 being open-ended at the first open end of the container and closed at the second open end of the container discuss slots 10a & 10b. The second piece of the container is a rigid ring 9a having a first end and a second end, where the rigid ring 9a is positioned over the first open end of the container so as to close the open end of the longitudinal slot. Preferably, one end of the ring is flush with one edge of slot 10b without blocking slot 10b. To help hold the ring 9a in position on the wall 9 of the first piece of the container, the ring has a circumferential ridge on its interior surface, and the container has a circumferential groove on its exterior surface near the first open end of the container (FIG. 20). The rigid ring fits over the first open end of the container until the circumferential ridge snaps into the circumferential groove. Additionally, the rigid ring may have a longitudinal ridge on its interior surface, where the longitudinal ridge fits into the open end of the longitudinal slot so as to prevent the ring from rotating relative to the wall 9.

FIG. 4 shows how the needle assembly of FIG. 1a is contained within the container of FIG. 2. The needle assembly is positioned within the container with pin 7 slidably engaging slot 10. Crosspiece 8 helps to retain pin 7 within slot 10. Piece 8 is sufficiently large that it cannot pass through slot 10 into the interior of the container, and is rigidly secured to a defined position along the length of pin 7, where the defined position on pin 7 is chosen so that hub 2 of the needle assembly is positioned along the cylindrical axis of the container, as shown in the cross-sectional view of FIG. 4. More particularly, the distance between the axis of hypodermic needle 1 and crosspiece 8 is equal to the one half the external diameter of the wall 9 of the container. This retains needle 1 along the axis of the container. Removal of knob 8 would allow pin 7 to slip out of slot 10, causing hub 2 to fall against the inside of wall 9. Ring 9a prevents pin 7 from exiting the open end of slot 10. As shown in FIG. 4, 9a is flush with one edge of slot 10a. In general, the size of the container can be chosen so as to accommodate any size syringe. Thus, if a large syringe is to be used, a container having a large interior diameter is required. The maximum diameter of the combination of hub 2 and sleeve 3 can be selected so as to correspond to the interior diameter of the container wall 9. Thus, a specific needle-holding assembly having a specific hub size may be manufactured for each commonly used syringe size. Alternatively, a standard-sized hub and sleeve may be used in each case, regardless of the size of the syringe and/or container. This may be done by varying the length of pin 7, so as to match the distance between sleeve 3 and the wall 9 of the container.

A needle having a hub of any desired size may be used in a container having any desired radius without losing the desired axial orientation of needle 1 by simply changing the distance between the axis of needle 1 and crosspiece 8. This makes it unnecessary to manufacture a wide variety of needle hubs, with each needle hub being reserved for a different container size, as required by D'Amico.

A spring 16 is also positioned within the container, as shown in FIG. 4. A first end of spring 16 engages ledge 15 at the second end of container 1, while the second end of spring 16 engages ledge 5 encircling hub 2. The spring acts to bias hub 2 away from the second end of the container so that needle 1 is effectively concealed within the container. This allows the user to effectively handle the assembly without pricking his fingers. Preferably, the tip of the needle bore is positioned inside 14 (FIG. 4).

When one is ready to use the needle, needle 1 may be exposed by pushing hub 2 toward the second end of the container. This is most easily done by manually sliding crosspiece 8, attached to pin 7, along slot 10 with the user's thumb or finger. As hub 2 approaches the second end of the container, spring 16 is compressed and needle 1 passes through opening 14 in the container and is exposed. Since needle 1 is directed along the axis of the container, it is very easy to direct the needle through opening 14. When pin 7 reaches end 12 of slot 10, the needle is rotated by reversibly pushing pin 7 into slot 10a. Slot 10a acts as a stop, preventing spring 16 from decompressing and causing needle 1 to retract into the container. An illustration of the needle assembly in this configuration is shown in FIG. 5. This has the great advantage that one may expose a sheathed needle without having to position one's fingers near the needle itself, as is done when exposing the sheathed needle described by Strauss (vide supra). When it is desired to retract the needle, 16 reversibly pushes pin 7 along slot 10 pin 7 out of slot 10a, and then spring.

As shown in FIGS. 1 through 5, slot 10a is a simple transverse slot which intersects slot 10 at a right angle. While this is an effective arrangement, other configurations of slot 10a are possible. Three such arrangements are shown in FIGS. 6a through 6c. In FIG. 6a, slot 10a is configured as a T-shaped notch. This T-shaped notch comprises a first transverse leg 10d which intersects slot 10, and a second leg 10e which intersects the transverse leg and is substantially parallel to slot 10. If desired, transverse leg 10d and leg 10e may be configured as an L-shaped notch, as shown in FIG. 6b. The notches of FIGS. 6a and 6b operate in the following manner. Hub 2 is moved forward within the container until pin 7 reaches end 12 of slot 10. At this point, the needle is rotated by pushing pin 7 into transverse leg 10d of slot 10a until the pin reaches the point where legs 10d and 10e intersect. At this point, spring 16 biases the hub 2 away from ridge 15, causing pin 7 to enter leg 10e of slot 10a. Leg 10e acts as a stop, preventing spring 16 from decompressing further and causing needle 1 to retract into the container. Leg 10e also prevents the user from accidentally pushing pin 7 out of slot 10a.

In FIG. 6c, slot 10a is configured as a C-shaped slot, where a first end of the C-shaped slot intersects slot 10 at point 12, and a second end 10d lies in line with slot 10. The end of slot 10 is separated from the second end of slot 10a by tab 24. The C-shaped configuration of slot 10a operates in the following manner. Hub 2 is moved forward within the container until pin 7 reaches end 12 of slot 10. At this point, the needle is rotated by pushing pin 7 along slot 10a until it reaches end 1d. At this point, spring 16 biases the hub 2 away from ridge 15, pressing pin 7 against tab 24. Tab 24 acts as a stop, preventing spring 16 from decompressing further and causing needle 1 to retract into the container.

Notch 10b, which intersects longitudinal slot 10 near the first end of the container, also functions as a locking mechanism When the needle is retracted into the container, pin 7 is adjacent to slot 10b. Pin 7 may then be pushed sideways into slot 10b so as to hold the needle assembly in the retracted position. Like slot 10a, slot 10b may be a straight transverse slot, a C-shaped slot, an L-shaped slot, or a T-shaped slot. Notches 10a and 10b are each wide enough to receive the pin engaged by the longitudinal slot. To retain pin 7 in notch 10a or in notch 10b when the needle is in use, each notch may be provided with teeth 200 which are spaced sufficiently closely together that the pin may not be pushed into, or out of, the notch without the deliberate application of force. A pair of such teeth are shown in the entrance to notch 10b in FIG. 7.

As shown in FIG. 6d, the means for reversibly locking the needle assembly in its exposed position may comprises a pair of teeth 200 on opposite sides of the longitudinal slot, said pair of teeth being positioned near a posterior end of the tubular sheath. No intersecting slots are required. A locking position is defined between the teeth and the posterior end of the longitudinal slot. The teeth cause the width of the slot to narrow to a width which is smaller than the diameter of the radially projecting member, but large enough to allow a user to push the radially projecting member through the teeth. A similar mechanism for reversibly locking the needle assembly in its retracted position comprises a pair of teeth on opposite sides of the longitudinal slot, said pair of teeth being positioned near an anterior end of the tubular sheath. Alternatively (FIG. 6e), teeth 200 may be positioned on opposite sides of a slot 10a which intersects slot 10 at a right angle.

As shown in FIG. 6f, the means for reversibly locking the needle assembly in its exposed position may comprises a first hook 220a which engages the radially projecting member 7, and the means for reversibly locking the needle assembly in its retracted position may comprise a second hook 220b (not shown in FIG. 6f) which engages the radially projecting member. The first hook is located at the posterior end of the longitudinal slot, and the second hook is located at the anterior end of the longitudinal slot. If radially projecting member 7 is substantially longer than it is wide (FIG. 6g), a notch 7a in an edge of member 7 may be used to assist in engaging a hook 220a or 220b. The hook fits into the notch 7a, stabilizing the position of the radially projecting member.

Preferably, since used syringe needles may be biohazards, the retractable syringe needle also includes a mechanism for irreversibly engaging the pin near the first end of the container so as to retain a used needle in the retracted position. One version of the irreversible locking mechanism comprises a third notch 10c which intersects longitudinal slot 10 so that slots 10b and 10c are collinear, extending from opposite sides of slot 10 (FIG. 7). Slot 10c is wide enough to receive the pin engaged by the longitudinal slot, and comprises a pair of flexible projections 10f extending from opposite sides of slot 10c. The projections have tips which contact each other, said tips being adapted to allow the pin engaged by the slot to pass therethrough when the pin enters the slot 10c from longitudinal slot 10, and to not allow the pin to pass therethrough to exit slot 10c. Each of the flexible projections makes an acute angle with the wall of slot 10c, and each of the flexible projections is directed away from the longitudinal slot 10. The pin 7 can pass between the projections as it enters slot 10c (FIG. 8b), but it cannot exit slot 10c between the projections (FIG. 8c). Projections 10f are able to bend away from slot 10 so as to allow pin 7 to pass therethrough and enter 10c, but they cannot bend toward slot 10 so as to allow pin 7 to exit 10c. If desired, one or more teeth 200 may be positioned in notch 10c between the opening to notch 10c and projections 10f although they are not required for proper functioning of the retractable syringe. Teeth 200, if present, are designed so that the pin may be reversibly pushed into notch 10c through the deliberate application of a force having at least a first defined magnitude. The projections 10f are preferably designed so that force of the first defined magnitude F.sub.1 is insufficient to force pin 7 through projections 10f Force of a second defined magnitude F.sub.2, greater than the first defined magnitude, is required to force pin 7 through projections 10f. Thus, the pin may be reversibly locked into notch 10c by pushing it into notch 10c with a force F, where F.sub.1.ltoreq.F<F.sub.2; and the pin may be irreversibly locked into notch 10c by pushing it into notch 10c with a force of F.sub.2 or greater. It is possible to omit notch 10b from the container structure entirely, and use notch 10c for both reversibly and irreversibly locking pin 7 into position. This is, however, much preferred to use notches 10b and 10c as separate locking mechanisms, due to the possibility of unintentionally irreversibly locking pin 7 into notch 10c when attempting to use notch 10c as a reversible lock.

A second version of the mechanism for irreversibly engaging the pin in its retracted position, shown in FIGS. 9a and 9b, comprises a radially-directed peg 300, said radially-directed peg being mounted on an exterior surface of the tubular sheath 9 so that one end of the radially-directed peg is adapted to be pushed inwardly through a hole 301 in the wall of the tubular sheath and through a hole 302 in the tubular sleeve 3. The radially directed peg may be mounted to the tubular sheath by means of a tubular mount 304 having a bore with a diameter that corresponds to the maximum outer diameter of peg 300 so that peg 300 slides axially within mount 304. Mount 304 is mounted to the side of sheath 9 so that the axis of the bore of the mount is normal to the axis of sheath 9, and so that the bore of mount 304 is positioned above hole 301 in sheath 9. Mount 304 may be secured to sheath 10 directly, or by means of a cap 305, as shown in FIGS. 9a and 9b. Cap 305 has a hole 305a therethrough, with this hole being in line with holes 301 in the tubular sheath. When pin 7 enters slot 10b and reversibly secures the needle assembly in a retracted position, hole 302 through the tubular sleeve in the needle assembly is brought into alignment with holes 305a and 301 (FIG. 9c; peg 300 omitted for clarity). Thus, after reversibly locking the needle in its retracted position, peg 300 can be simultaneously pushed through holes 305a, 301, and 302, preventing movement of hub 2 relative to sheath 9. If the needle has not been reversibly locked, hole 302 is not aligned with holes 305a and 301, preventing peg 300 from engaging hole 302 in the tubular sleeve (FIG. 9d; peg 300 omitted for clarity). Holes 305a and 301 may have a larger diameter than hole 302. Preferably, a stop 306 on peg 300 limits the depth to which peg 300 can enter sleeve 3. The outer diameter of stop 306 is greater than the diameter of hole 302. After the end of the radially-directed peg 300 is pushed through hole 302, peg 300 may not be withdrawn through the hole in the tubular sleeve. This is due to flexible projection or projections 303, which project radially from peg 300. Projections 303 are angled toward stop 306, and away from the axis of sheath 9. Before peg 300 is pushed through holes 305a, 301, and 302 (FIG. 9b, the unlocked configuration), projections 303 are restrained to lie against peg 300 by the wall of mount 204. After peg 300 is pushed through hole 302 (FIG. 9a, the locked configuration), projections 303 are no longer restrained and extend radially. Since they are angled toward the interior of the wall of sleeve 3, projections 303 cannot be readily be folded away from the wall of sleeve 3. This makes it difficult or impossible to withdraw peg 300, resulting in a permanent lock.

Mount 304 will now be described in more detail. Mount 304 preferably is manufactured as a first inner cylindrical tube 304a and an outer cylindrical tube 304b. Tube 304a has an inner diameter which is equal to the diameter of holes 301 and 305a. Tube 304b has an inner diameter which is equal to the outer diameter of tube 304a, and an inwardly projecting flange 304c at one end. Flange 304c defines a hole 304d having a diameter which is large enough to allow the outer end of peg 300 to reversibly slide therethrough, but which is small enough to prevent stop 306 from passing therethrough. An exploded view of this construction is shown in FIG. 9f. Tubes 304a and 304b are preferably ultrasonically welded to ring 305. If a simplified construction is desired, tube 304a may be omitted and the inner diameter of tube 304b may be set to be equal to the diameter of holes 301 and 305a. This allows mount 304 to be constructed from a single piece.

If desired, projection 303 may take the form of a frusto-conical tube made of a flexible material (FIG. 9e). The narrow end of the frusto-conical tube is rigidly fixed to the inwardly directed end of peg 300. The frusto-conical tube is coaxial with peg 300, and surrounds the inwardly directed end of peg 300, with the proviso that the overall length of the frusto-conical tube is less than the distance between the inwardly directed end of peg 300 and stop 306. When peg 300 is simultaneously pushed through holes 305a, 301, and 302, the sides of the frusto-conical tube collapse against the side of peg 300. After the peg and the frusto-conical tube attached thereto are pushed through hole 302, the sides of the frusto-conical tube expand. Since the large end of the frusto-conical tube has a diameter that is greater than the diameter of hole 302, peg 300 may not be withdrawn through the hole in the tubular sleeve.

In an alternative embodiment, projections or tube 303 may be rigid and non-flexible. If 303 is non-flexible, hole 302 should have a smaller diameter than the maximum diameter of tube 303 or the maximum distance across projections 303. After the projections or tube 303 penetrate hole 302, the upper ends of projections or tube 303 act as stops to prevent the peg 300 from being withdrawn through the hole in the tubular sleeve.

A third version of the mechanism for irreversibly engaging the pin at the second defined location in said longitudinal slot so as to hold said needle assembly in a position where the needle is retracted within the container is provided. This version of the mechanism features the rigid ring 9a mounted on wall 9 of the container; and a rigid tongue 9b attached to one end of the rigid ring by a living hinge 9c (FIG. 10a). This tongue is positioned so that it extends from the end of the container with syringe barrel-receiving opening 13. The second end of the rigid ring is substantially flush with one side of the slot 10b, without blocking slot 10b (slot 10c is not present in this embodiment). To permanently lock the needle assembly in a retracted position, pin 7 is moved into slot 10b, exactly as for the procedure for reversibly locking pin 7 into position. The rigid tongue is folded in the direction of arrow A against the external surface of the ring and irreversibly secured against the external surface of the ring so that the end of the rigid tongue blocks the opening of slot 10b while pin 7 is inside slot 10b. To accomplish this, the tongue is preferably designed so that it is collinear with slot 10 when it is in its initial, unfolded state, and has a length which is at least equal to the sum of the longitudinal length of the rigid ring and the width of slot 10b. To secure the tongue against the external surface of the ring, a hook 9d on the rigid tongue irreversibly snaps around the second end of the rigid ring (FIG. 10b). Hook 9d also blocks the opening to slot 10b. Alternatively, a post 9e on the rigid tongue may irreversibly snap into a hole 9f in the external surface of the rigid ring (FIG. 10c). A projection on the end of the rigid tongue fits into slot 10, blocking the opening to slot 10b (FIG. 10d).

One difficulty in manufacturing an article of this type lies in the difficulty in getting the pin on the needle assembly to properly engage slot 10. For example, the invention of D'Amico (vide supra) presents a substantially cylindrical hub having a radially protruding pin attached thereto positioned within a tubular container. The inner circumference of the container is substantially the same as the outer circumference of the hub. The pin is positioned within a slot in the wall of the container, where each end of the slot is closed. However, this article is difficult to manufacture inexpensively. When the hub slides into the container, the radially protruding pin is blocked by the end of the tubular container wall, and cannot readily enter the container.

This invention attempts to solve this problem. When the container is manufactured in one piece with a slot 10 which is closed at both ends, the combination of pin 7 and crosspiece 8 will not pass through slot 10 when the needle assembly of FIG. 1a is positioned inside the container of FIG. 2. To overcome this difficulty, one can position the needle assembly inside the container prior to attaching pin 7, and then insert pin 7 through slot 10 and secure the pin to sleeve 3. Alternatively, the container may be manufactured in two pieces, a tubular container and rigid ring 9a.

The retractable syringe needle of the current invention may be made by obtaining a needle assembly as previously described, and obtaining the previously-described container having a tubular wall 9 with an open-ended longitudinal slot 10 therein (FIG. 11). A spring or other biasing means is then inserted into the container. The needle assembly is then inserted into the syringe barrel-receiving end of the container so that pin 7 enters the open end of slot 10, and is slidably engaged by the longitudinal slot. The biasing means engages the hub of the needle assembly and reversibly biases the needle assembly toward a first position where the needle is concealed within the container. The rigid ring is then mounted on the container so that the ring closes the open end of slot 10, preventing the pin 7 from exiting slot 10.

A second, and less preferred, method of solving the problem involves formation of the container in two parts, as shown in FIG. 12. The container is formed from an anterior portion 20 and a posterior portion 21. Anterior portion 20 has a first open end adapted to receive a syringe barrel and a second open end adapted to receive a hypodermic needle. Ridge 15 is positioned on the interior surface of the wall of anterior container portion 20. A first longitudinal slot 22 runs from the first end of the anterior portion of the container to point 12, near the second end of the anterior portion of the container. Slot 10a meets slot 22 at a right angle. Posterior portion 21 of the container has a first open end adapted to receive a syringe barrel and a second open end adapted to receive a syringe barrel. A second longitudinal slot 23 runs from the first end of the posterior portion of the container to point 11, near the second end of the posterior portion of the container. The first end of and the first end of 21 are adapted to be joined together to form the complete container, by attaching 20 and 21 together so that slots 22 and 23 cooperate to form slot 10.

The manner in which 20 and 21 are joined together is not particularly limited. Parts 20 and 21 may be bonded together by means of a biocompatible adhesive. Alternatively, threaded ends on 20 and 21 may be screwed together, and then secured with a suitable adhesive. Also, a ridge on an interior surface of one piece may snap into a groove on an exterior surface of another piece. The ridge may be treated with an adhesive prior to snapping it into the groove. Finally, if 20 and 21 are made from a thermoplastic material (i.e., polyolefin), they may be heat-sealed together. In the embodiment illustrated in FIG. 12, a threaded end 20a on container portion 20 is screwed onto a threaded end 21a on container portion 21.

The complete assembly is manufactured in the following manner, shown in FIG. 13. A spring 16 and the needle assembly are joined together by joining a first end of the spring to ridge 5 on hub 2. The needle 1 is positioned along the helical axis of the spring. This assembly is then positioned within the anterior portion 20 of the container so that a second end of the spring engages ridge 15. Container portion 20 is then joined to container portion 21 so that: a) slots 22 and 23 line up to form slot 10; and b) pin 7 is slidably engaged by slot 10.

Alternatively, hub 2 may be positioned within posterior portion 21 so that pin 7 engages slot 23, and then part 20 may be joined to part 21 of the container so that the second end of the spring engages ridge 15. Again, when joining pieces 20 and 21, care should be taken to ensure that slots 22 and 23 are aligned so as to form a single slot 10 which engages pin 7.

This assembly method allows the safety needle to be assembled quickly and easily, and avoids the difficulty of trying to position the needle inside a fully assembled container without damaging the pin by forcing it past the rim of the container.

FIGS. 14 and 15 illustrate use of a syringe assembly with the safety needle of FIG. 3. The syringe comprises a syringe barrel 17, and a syringe plunger 18 slidably mounted therein. Barrel 17 has a frusto-conical tip 19 adapted to enter cavity 6 of sleeve 19 (cavity 6 is not shown in FIGS. 5 and 6, as it is occupied by tip 19.). Tip 19, after insertion into cavity 6, frictionally engages the interior of sleeve 3, forming a leakproof seal. A hole in tip 19 receives fluids which have passed through the bore of needle 1.

As shown in FIG. 15, syringe barrel 17 may be used to push the needle assembly within the container toward the second end of the container, compressing the spring and causing needle 1 to emerge through hole 14. In this position, the container encases at least a portion of barrel 17. Barrel 17 may then be rotated, causing sleeve 3 to rotate. This causes pin 7 to enter slot 10a, locking the syringe needle into position. The assembled syringe, with the needle exposed, may then be used to take a sample of a fluid. More particularly, the assembled syringe may be used to administer an injection to a patient, or to take a sample of arterial or venous blood from a patient.

After use, the contaminated needle may be discarded by rotating barrel 17 in the reverse direction to free pin 7 from slot 10a. This allows spring 16 to decompress, causing the container to slide forward off of the syringe barrel and cover needle 1. The syringe barrel may then be separated from sleeve 3, and the container with the needle concealed therein may be discarded with minimal risk of injury from contact with the contaminated needle. The syringe barrel and plunger may be discarded, or sterilized in an autoclave for reuse.

As shown in FIG. 16, it is possible to secure two pins 7, each having a crosspiece 8 mounted thereto, on a single needle assembly, where the two pins are directed in opposite directions. Such a needle assembly may be mounted in a container having two slots 10a in opposite sides of wall 9. A transverse slot 10a intersects each slot 10, with each slot 10a running in the same direction (i.e., either clockwise or counterclockwise, when viewed from the second end of the container along the container axis). This version of the apparatus operates in the same manner as the assembled apparatus of FIG. 3. The only difference is that the presence of the second pin anchors hub 2 of the needle assembly more fully along the axis of the container (FIG. 17).

FIG. 18 shows an alternative embodiment of the needle assembly of FIG. 1a. This embodiment of the needle assembly features a hollow straight needle 29 having two ends. The needle 29 extends through a hub 30, so that a first end of the needle 29a points in a forward direction, and a second end of the needle 29b points in a reverse direction. Pin 7 is rigidly connected with said hub, and extends in a radial direction. Crosspiece 8 is connected with the pin at a defined distance from the hub. Preferably, a rubber sheath 31 covers end 29b of needle 1.

FIG. 19 shows the needle assembly of FIG. 18 mounted within a container similar to that of FIG. 2. The container features a defined cylindrical axis and has a tubular wall 9 with a longitudinal slot 10 therein. A first open end of the container is adapted to receive a receptacle for venous blood, preferably an evacuated test tube with a rubber stopper, and a second open end adapted to allow the first end of the hollow needle to pass therethrough. The longitudinal slot extends from the first open end of the container to a defined point near the second open end of the container, where the longitudinal slot is open-ended at the first open end of the container and closed at the second open end of the container. A rigid ring is positioned over the first open end of the container so as to close the open end of the longitudinal slot. A plurality of circumferential strengthening ridges may be positioned on the exterior surface of the container. The needle assembly is mounted within the container so that (i) the first end of the needle, 29a, is directed toward the second open end of the container, and (ii) pin 7 on the needle assembly is slidably engaged by longitudinal slot 10, with crosspiece 8 acting to support hub 30 so that it is positioned on the axis of the container. End 29a of needle 29 is exposed by using the thumb or finger to manually slide piece 8 forward toward needle-receiving opening 14, carrying hub 30 toward the second end of the container until the needle end 29a passes through opening 14 and is exposed. Piece 8 is then pushed sideways until pin 7 enters slot 10a, locking the needle into the exposed position. The needle may then be inserted into a patient's blood vessel. The rubber sheath prevents the patient's blood from traveling through the needle. Positioned inside the container, there is a spring or other means for biasing the needle assembly towards a position where the needle is concealed inside the container; the biasing means acts to prevent premature exposure of the needle.

The double-ended safety needle additionally features a first notch 10a which intersects the longitudinal slot at a first defined location near the needle-receiving opening 14 in the container. The needle may be reversibly secured in an exposed position by pushing pin 7 toward opening 14 until pin 7 is positioned adjacent to notch 10a, and then pushing pin 10b sideways into notch 10a. The biasing means presses the pin against the rear wall of notch 10a, securing the needle assembly into position. Similarly, the needle may be reversibly secured in a concealed position by pushing pin 7 toward opening 13 until pin 7 is positioned adjacent to a second notch 10b near opening 13 in the container, and then pushing pin 10b sideways into notch 10b. As previously described, each of notches 10a and 10b may be straight transverse notches, or notches 10a and 10b may each independently be a T-shaped notch (as seen in FIG. 6a), a L-shaped notch (FIG. 6b), or a C-shaped notch (FIG. 6c). Also, each notch may be provided with teeth 200 which are spaced sufficiently closely together that the pin may not be pushed into, or out of, the notch without the deliberate application of force.

A means for irreversibly engaging the needle assembly in a retracted position comprises a third notch 10c, where notches 10b and 10c are collinear and extend in opposite directions from the longitudinal slot as seen in FIGS. 7 and 8. A pair of flexible projections having tips which contact each other extend from opposite sides of notch 10c. The tips are adapted to allow the pin engaged by the slot to pass therethrough when the pin enters notch 10c from the longitudinal slot, and to not allow the pin to pass therethrough to exit notch 10c.

Alternatively, the means for irreversibly engaging the pin may comprise a radially projecting peg 300 which is secured to the rigid ring by a tubular mount 304, substantially as seen in FIGS. 9a and 9b. The tubular mount preferably takes the form of a cylinder having a defined axis, where the defined axis of the cylinder is directed radially outward from the surface of the housing. The rigid ring is positioned so that one end of the rigid ring is substantially flush with one side of notch 10b (no notch 10c is present in this embodiment). To secure the pin in notch 10b, the peg is pushed through a series of coaxial holes 305a, 301, and 302, through the ring, the sheath 9, and the sleeve 3, respectively. Projections 303 on peg 300 then spread out and prevent peg 300 from being withdrawn through hole 302, effectively locking the needle assembly in place, relative to sleeve 9. The peg must be short enough that it will not interfere with the rearwardly projecting end of the hollow needle.

Additionally, the means for irreversibly engaging the pin may comprise a rigid tongue attached to one end of the rigid ring by a living hinge, as seen in FIGS. 10a through 10d. The rigid ring is positioned so that the other end of the rigid ring is substantially flush with one side of notch 10b (no notch 10c is present in this embodiment). To secure the pin in notch 10b, the rigid tongue is folded against an external surface of the ring and irreversibly secured against the external surface of the ring so that the end of the rigid tongue blocks the opening of the second notch.

To hold the rigid ring in position relative to the wall of the container, a circumferential ridge 9g on the interior surface of the rigid ring 9a snaps into a circumferential groove 9h on the exterior surface of the container (FIG. 20). Also, a ridge 9i on the interior of the rigid ring may fit into the open end of slot 10 to prevent rotation of the ring relative to the slot.

The assembly of FIG. 19 may be used with a receptacle for receiving a blood sample, as shown in FIG. 21. This receptacle is a test tube 32 having an open end. A rubber septum 33 seals the open end of the test tube. The interior of the test tube may be under vacuum While needle 29 is in the patient's blood vessel, the end of the test tube which is sealed by septum 33 is inserted into opening 13 of the container until septum 33 contacts rubber sheath 31. The test tube is then pushed toward hub 30, and septum 33 pushes the end of rubber sheath 31 along needle 29 toward hub 30, exposing end 29b of needle 29. End 29b of needle 29 pierces the rubber sheath 31 and septum 33, entering the test tube. Blood from the patient then travels through hollow needle 29 into the test tube. After taking a sample of the patient's blood, test tube 32 is removed from the container. Rubber sheath 31 resumes its original configuration, covering end 29b of the needle and cutting off the flow of blood. Needle 29 is then withdrawn from the patient's blood vessel. Crosspiece 8 is then pushed sideways until pin 7 exits slot 10a, unlocking the needle. Spring 16 then causes needle 1 to withdraw into the container.

As in the syringe needle assembly of FIG. 3, piece 8 is sufficiently large that it cannot pass through slot 10 into the interior of the container, and is rigidly secured to a defined position along the length of pin 7, where the defined position on pin 7 is chosen so that hub 30 of the needle assembly is positioned along the cylindrical axis of the container. More particularly, the distance between the axis of hypodermic needle 1 and crosspiece 8 is equal to the one half the external diameter of the wall 9 of the container. This retains needle 29 along the axis of the container.

The use of crosspiece 8 to retain needle 1 in position is particularly important in an apparatus for obtaining blood samples. The container has to be wide enough to receive the test tube, which in turn is normally wider than hub 2. Without crosspiece 8, pin 7 would slip out of slot 10, and end 29b of needle 29 would fall against the inner surface of wall 9. Needle 29b would then be incorrectly positioned to penetrate septum 33.

A threaded male joint 34 may surround opening 13 at the first end of the container of FIG. 2, and a threaded male joint 35 may surround opening 14 at the second end of the container. Cap 36 having a threaded female joint may be screwed onto joint 34, covering opening 13, and cap 37 having a threaded female joint may be screwed onto joint 35, covering opening 14. This is normally done whenever the needle is not intended to be exposed, so as to minimize the risk of accidental contact with the tip of the needle.

A further embodiment of the invention will now be discussed. This embodiment, shown in FIG. 22, features a hollow hypodermic needle 38 and a cylindrical hub 39 having an axial passage therethrough. The hollow needle is rigidly connected with the hub so that the a