Patella 38mm, REF164-0038 Product Usage: UHMWPE component used in a TKA procedure to resurface the patella and serve as a bearing surface for sliding contact with the femoral component
FDA Recall Z-2254-2014 · Posted 2014-08-17
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Reason for Recall
Firm Action
Root Cause
Packaging process control
Distribution Pattern
Worldwide Distribution - US Nationwide and the country of Japan. No military/govt/VA consignees.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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