Date Initiated by Firm | February 22, 2008 |
Date Posted | September 16, 2008 |
Recall Status1 |
Terminated 3 on October 25, 2010 |
Recall Number | Z-1626-2008 |
Recall Event ID |
46963 |
Product Classification |
Screwdriver - Product Code HXX
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Product | Gamma 3 System Set Screwdriver, Flexible Shaft; 4mm, This product is non-sterile Stryker Trauma GmbH, Germany; Distributed by Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430 - Orthopedic Device. The Gamma3 Locking Nail Systems are intramedullary short and long fixation nails intended for control of rotation and shortening of fractured femurs. The screwdriver is used to place the set screw in the nail. |
Code Information |
Product number: 1320-0231 Lot Code on Package label K409181, Lot code engraved on Screwdriver: K968226; Lot code on package label: K610297, Lot code engraved on Screwdriver: K782153; Lot code on package label; K645667, Lot code engraved on screwdriver: K533686; Lot code on package label: K688034, Lot code engraved on screwdriver: K887079; and Lot code on package label: K878962, Lot code engraved on screwdriver: K533686. |
Recalling Firm/ Manufacturer |
Stryker Howmedica Osteonics Corp. 325 Corporate Dr Mahwah NJ 07430-2002
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For Additional Information Contact | Rita Intorella 201-831-5825 |
Manufacturer Reason for Recall | Stryker Trauma has become aware that five lots of the Gamma3 Set Screwdriver have hexagon tips that were not hardened to specification. If the screwdriver tip were to deform intra-operatively, the correct positioning of the set screw would not be possible, which could lead to lateral or medial migration of the lag-screw. |
FDA Determined Cause 2 | Finished device change control |
Action | On February 22, 2008 Urgent Product Recall notification letters were sent to Stryker Branches/Agencies, Risk Management Departments at hospitals and surgeons via Federal Express. If you have any questions contact Rita Intorrella at (201) 831-5825 or the Hip Fracture Team at (201) 831-5291. |
Quantity in Commerce | 43 total (single and kits) |
Distribution | Class II Recall - Nationwide Distribution. |
Total Product Life Cycle | TPLC Device Report |
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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