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Class 2 Device Recall Nail Holding Screw |
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Date Initiated by Firm |
August 30, 2010 |
Date Posted |
November 09, 2010 |
Recall Status1 |
Terminated 3 on August 21, 2012 |
Recall Number |
Z-0331-2011 |
Recall Event ID |
56800 |
Product Classification |
Rod, fixation, intramedullary and accessories - Product Code HSB
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Product |
Nail Holding Screw; 1 unit per package Stryker Trauma GmbH; Distributed by Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430 The nail holding Screw is used to assemble the nail to the target device. The Nail holding Screw is further the mating part (inner thread) of the External Compression Device as the instruments needs to be threaded into the Nail holding Screw in order to achieve Compression at the fracture side. |
Code Information |
Catalog Number: 1806-1602; Lot codes: K101924, K240627. |
Recalling Firm/ Manufacturer |
Stryker Howmedica Osteonics Corp. 325 Corporate Drive Mahwah NJ 07430
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For Additional Information Contact |
Richard Wolyn 201-972-2100
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Manufacturer Reason for Recall |
Variations in the outer diameter of the shaft of the External Compression Device and the inner diameter of the Nail Holding Screw may make assembly of these 2 instruments not possible.
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FDA Determined Cause 2 |
Other |
Action |
Stryker sent Recall notification letters by Federal Express on September 9, 2010 to all Stryker branches/agencies and Risk Managers, Chief of Orthopaedics of affected hospitals and Surgeons on September 10, 2010, that used the product. The letter identified the product, the problem, and the action that customers should take.
Customers were instructed to:
Examine their inventory and hospital locations to identify the affected product and return it to their branch or agency warehouse for reconciliation.
Reconcile all product on the attached Product Recall Acknowledgment Form and fax a copy to (201) 831-6069 within 5 days of receipt of notice.
A Stryker representative would contact the customer with details for return of the product.
For any questions regarding this recall call (201) 972-2100. |
Quantity in Commerce |
22 |
Distribution |
Nationwide Distribution including AZ, CA, CO, FL, GA, IL, KY, MD, OH, OK, and TX |
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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