Date Initiated by Firm | August 27, 2012 |
Date Posted | November 20, 2012 |
Recall Status1 |
Terminated 3 on August 27, 2013 |
Recall Number | Z-0386-2013 |
Recall Event ID |
63126 |
510(K)Number | K071718 |
Product Classification |
Prosthesis, hip, constrained, cemented or uncemented, metal/polymer - Product Code KWZ
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Product | Trilogy II Constrained Liner
The Trilogy Longevity Constrained Liner serves as the articular surface for a femoral head in total hip arthroplasty. |
Code Information |
Item 00-6334-062-36, Lot 62023769 |
Recalling Firm/ Manufacturer |
Zimmer, Inc. 345 E Main St Warsaw IN 46580-2746
|
For Additional Information Contact | Dona Reust 574-372-4807 |
Manufacturer Reason for Recall | Trilogy Longevity Constrained Liner devices were packaged in incorrect cartons. The product is packaged in the incorrect carton. Product labels and patient labels are correct, matching the product inside the carton. |
FDA Determined Cause 2 | Labeling Change Control |
Action | Zimmer contacted their customer beginning the week of August 27, 2012, via telephone. Zimmer informed the customer the reason of the recall.
The customer was instructed to quarantine and return the device to Zimmer Product Service, 1777 W. Center St. Warsaw, IN 46580. The customer was asked to provide information if the product was further distributed.
For further questions please call 574-372-4316. |
Quantity in Commerce | 1 |
Distribution | USA (nationwide) including the states of Ohio, Carolinas and New England. |
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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510(K) Database | 510(K)s with Product Code = KWZ
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