Retractable Needle Syringe Assembly

• US 20080097308A1
• Filed: 08/12/2005
• Published: 04/24/2008
• Est. Priority Date: 08/13/2004
• Status: Active Grant

• Current Assignee: Becton, Dickinson & Co
• Original Assignee: Becton, Dickinson & Co
• Inventors: Schiller, Eric R., Paddock, Douglas, D'Arrigo, Christina J.
• Granted Patent: US 7,988,663 B2
• Time in Patent Office: Days
• US Class Current: 604/110
• CPC Class Codes: A61M 5/3234 Fully automatic needle retraction, i.e. in which triggering of the needle does not require a deliberate action by the user
• CPC Class Codes: A61M 5/347 rotatable, e.g. bayonet or screw A61M5/344 takes precedence
• CPC Class Codes: A61M 5/508 Means for preventing re-use by disrupting the piston seal, e.g. by puncturing

Abstract

A syringe including a barrel (14), a retractable needle (12) and a plunger rod assembly (22) including inner (30) and outer (24) members with a stopper (46) for expelling fluids from the syringe is disclosed. An activation member (40, 44) associated with the plunger rod permits relative movement of the inner and outer members when activated. The stopper is configured to compress a sufficient amount when advanced distally in the barrel to cause the activation element to engage and cause retraction of the needle within the syringe.

Claims

1. A syringe including a retractable needle comprising:

a barrel having a fluid chamber defining a longitudinal axis and including a proximal end, and a distal end adapted to be attached to a needle;

a plunger rod having a distal end and proximal end, the plunger rod including an inner sleeve slidably engageable with an outer housing, the inner and outer housing being axially moveable with respect to each other upon activation of a decoupling element associated with the plunger rod; and

a compressible stopper mounted on the distal end of the of the plunger rod, the stopper being configured such that when distal force is applied to the plunger rod, the stopper is compressed in the direction of the longitudinal axis in an amount to allow distal movement of the plunger rod along the longitudinal axis a distance sufficient to permit activation of the decoupling element, causing the inner sleeve to decouple from the outer housing and move distally with respect to the outer housing and retraction of the needle within the syringe barrel.

2. The syringe of claim 1, wherein activation of the decoupling element is dependent upon both compression of the stopper and distal displacement of the plunger rod along the longitudinal axis.

3. The syringe of claim 1, wherein the stopper includes an outer wall portion including a distal rib spaced from a proximal rib defining a gap region in the outer wall, the gap region having a wall thickness that is less than the wall thickness of the proximal rib and the distal rib.

4. The syringe of claim 3, wherein the barrel includes and inner surface and a ceiling located adjacent the distal end on the inner surface to engage the distal rib when the plunger rod is advanced distally within the chamber.

5. The syringe of claim 1, wherein the stopper has an axial length and a diameter, and the axial length of the stopper is at least about 50% of the diameter of the stopper.

6. The syringe of claim 4, wherein the axial length of the stopper is at least equal to the diameter of the stopper.

7. The syringe of claim 1, wherein the inner sleeve and the outer housing are configured such that at least about 26 pounds of distal force can be applied to the plunger rod without decoupling of the inner sleeve and outer housing.

8. The syringe of claim 7, wherein activation element includes a flexible finger formed on the inner sleeve, the flexible finger including a distal end and the outer sleeve includes a wall with a window formed adjacent the proximal end of the plunger rod, the window including a distal end and a proximal end, the finger and the window being sized so that the finger fits within the window and the distal end of the finger engages the distal end of the window to prevent distal axial movement of the inner sleeve with respect to the outer housing when distal pressure is applied to the plunger rod.

9. The syringe of claim 9, wherein the barrel includes an inner surface and a shoulder formed on the inner surface adjacent the proximal end adapted to engage the contact surface, causing the finger to flex inwardly and permit relative distal movement between the outer housing and inner sleeve.

10. The syringe of claim 9, wherein the contact surface is a ramped surface.

11. The syringe of claim 9, wherein the inner sleeve further includes a proximal facing edge adapted to engage the outer housing to prevent proximal movement of the inner sleeve relative to the outer housing.

12. A syringe comprising:

a barrel having a fluid chamber, an inside surface, a proximal end, a proximal shoulder located on the inside surface, a distal end adapted to be attached to a needle and a ceiling located on the inside surface and adjacent the distal end; and

a plunger rod having a distal end and a proximal end, the plunger rod adapted to slidingly engage the inside surface of the fluid chamber, the plunger rod including a hollow outer housing defined by a wall and a hollow inner sleeve slidably receivable within the outer housing and defining a cavity, and a stopper located on the distal end of the plunger rod, the stopper including a distal face and an outer wall surface, the outer housing including at least one window extending axially through the wall adjacent the proximal end of the plunger rod, the inner sleeve including at least one flexible finger adapted to be flexed inwardly towards the cavity, the flexible finger including a distal end, a proximal end, a distal facing ramp surface adapted to engage with the shoulder of the barrel and a distal facing edge, the inner sleeve further including a proximal facing stop edge, the finger being sized and shaped to be received within the window, the stopper including a distal rib, a proximal rib and a gap region between the ribs located along the outer wall surface, wherein the configuration of the ramp surface and the stopper is such that axial compression of the stopper permits sufficient axial movement of the plunger rod so that ramp surface engages the shoulder of the barrel, causing inward deflection of the fingers and relative movement of the inner sleeve and outer housing and retraction of the needle.

13. The syringe of claim 12, wherein the at least one window includes a distal end adapted to engage the distal facing edge of the finger to prevent relative distal axial movement of the inner sleeve and outer housing when distal force is applied to the plunger rod.

14. The syringe of claim 13, wherein the finger and distal edge are configured to withstand at least about 26 pounds of distally directed force.

15. The syringe of claim 13, the inner sleeve further including at least one lug located adjacent the proximal end of the plunger rod, the lug sized to fit within a track formed in the wall of the outer housing adjacent the proximal end, the lug including a proximal facing stop edge adapted to engage the housing to proximal movement of the inner sleeve with respect to the outer housing when proximal force is applied to the plunger rod.

16. The syringe of claim 15, wherein the inner sleeve includes a pair of fingers adapted to be deflected inwardly upon contact with the shoulder, the outer housing includes a pair of windows adapted to receive the pair of fingers, the inner sleeve further includes a pair of lugs, and the outer section includes a pair of tracks adapted to receive the lugs.

17. The syringe of claim 16, further comprising a pair of bosses formed on the inner sleeve and a pair of channels that cooperate to align the fingers with the windows and the lugs with the tracks.

18. The syringe of claim 17, wherein the pair of bosses are asymmetrical.

19. The syringe of claim 17, wherein one of the pair of bosses are offset from a centerline of the inner sleeve.

20. The syringe of claim 15, wherein the inner sleeve includes a cutting element mounted on the distal end.

21. The syringe of claim 19, wherein the outer housing includes webbing on the distal end adapted to support the end of the stopper as the stopper is advanced in a distal direction and a needle attached to the distal end of the barrel, the needle attached to a hub including a flange.

22. The syringe of claim 19, wherein inner deflection of the fingers permits distal movement of the inner sleeve within the outer housing, causing the cutting element to cut through the webbing, the stopper and the flange, causing the needle to retract within the barrel.

23. The syringe of claim 19, wherein the stopper includes a distal face, and when the stopper is advanced against the roof of the barrel, only a portion of distal face is contact with the ceiling of the barrel.

24. A syringe including a retractable needle comprising:

a barrel including a distal end, a proximal end, an inner surface and an engagement surface;

a plunger rod having a proximal end a distal end, the plunger rod adapted to be slidably received within the inner surface of the barrel, the plunger rod including an outer member and an inner member sized and configured to be slidably received within the inner member when an activation element is in contact with the engagement surface, the activation element including a flexible member associated with the inner member in contact with the outer member to prevent relative distal movement between the inner and outer members; and

a stopper on the distal end of the plunger rod configured to permit axial movement sufficient to allow displacement of the plunger rod to permit the engagement element to contact the activation surface when the stopper is engaged against the distal end of the barrel.