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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 22 of 22 Results
PMA Number: P010014
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FDA Recall
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Oxford Femoral Knee System REF 154600, LOT 2272736, WARNING DO NOT RESTERILIZE, STERILE UNLESS PACK ... 2 06/29/2011 Biomet U.K., Ltd.
Biomet Oxford Unicompartmental Knee, Phase 3, Right Medical Tibial Tray, Standard Size B, CoCr, ster... 2 02/03/2009 Biomet, Inc.
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