| Class 2 Device Recall Foundation Hip System Bipolar Modular |  |
Date Initiated by Firm | August 02, 2007 |
Date Posted | November 07, 2007 |
Recall Status1 |
Terminated 3 on January 09, 2008 |
Recall Number | Z-0096-2008 |
Recall Event ID |
44788 |
510(K)Number | K953510 |
Product Classification |
hip prosthesis - Product Code KWY
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Product | Foundation Hip System Bipolar Modular, Size 54mm OD; Cat. #412-01-054; Sterile; assembly required by physician prior to implant; manufactured by Encore Medical, L.P., Austin, TX 78758. |
Code Information |
Lot #: 608031, 648321, 675931, 678951, 678961, 678971, 695091, 695851, 780401, 788581, 788591, 788601, 794461, 831021, 840371, 844651, 848711, 855031, 857811, 875551, 894361, 894371, 907281, 933941, 949601, 964501 and 964511. |
Recalling Firm/ Manufacturer |
Encore Medical, Lp 9800 Metric Blvd Austin TX 78758
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For Additional Information Contact | 512-834-6235 |
Manufacturer Reason for Recall | Device mislabeled; hip prosthesis components validated for 5 years were labeled as having a 6 year expiration date. |
FDA Determined Cause 2 | Packaging change control |
Action | Firm notified consignees of recall via phone, e-mail and overnight letters beginning on 08/02/07. Consignees asked to return devices for a properly labeled replacement. |
Quantity in Commerce | 137 units. |
Distribution | Worldwide, including USA, Greece, Japan, and Saudi Arabia. |
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 = KWY
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