Pivot Bipolar Cup 22x42/43-51/53mm, REF 133-YYYY Product Usage: Used in a hemiarthroplasty procedure as the bearing surface to articulate with both the CoCr femoral head and the natural acetabulum
FDA Recall Z-2253-2014 · 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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