Date Initiated by Firm | November 20, 2013 |
Date Posted | February 10, 2014 |
Recall Status1 |
Terminated 3 on October 13, 2016 |
Recall Number | Z-0964-2014 |
Recall Event ID |
67234 |
Product Classification |
Orthopedic manual surgical instrument - Product Code LXH
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Product | Stryker Orthopaedics Navigation Compatible Accolade Broach Handle
1 single unit to a package
Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430 USA
Stryker France ZAC Satolas Green Pusignan Av de Satolas Green 69881 Meyzieu Cedex France
Made in USA
non-sterile |
Code Information |
Catalog no. 2124-1400 All lots |
Recalling Firm/ Manufacturer |
Stryker Howmedica Osteonics Corp. 325 Corporate Dr Mahwah NJ 07430-2002
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For Additional Information Contact | Ms. Colleen O'Meara 201-972-2100 |
Manufacturer Reason for Recall | Stryker received reports from the field of the impaction plate dissociating/fracturing from the main body of the broach handle. |
FDA Determined Cause 2 | Process design |
Action | Stryker Orthopaedics sent notification letters and acknowledgement forms via Fed Ex as follows:
Branches-11/20/2013
Hospital Risk Manager - 11/21/2013 |
Quantity in Commerce | 211 units |
Distribution | IL MA, MN, ND, OR, & PA |
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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