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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 19 of 19 Results
510(K) Number: K960279
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FDA Recall
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Zimmer, NexGen Complete Knee Solution LPS Flex Gender Femoral Component, Size E Left, sterile, REF 0... 2 12/02/2010 Zimmer Inc.
Zimmer, NexGen Complete Knee Solution LPS Flex Gender Femoral Component, Size F Right, sterile, REF ... 2 12/02/2010 Zimmer Inc.
Zimmer, NexGen Complete Knee Solution LPS Flex Gender Femoral Component, Size G Left, sterile, REF 0... 2 12/02/2010 Zimmer Inc.
Zimmer, NexGen Complete Knee Solution LPS Femoral Component, Size E Right, sterile, REF 00-5996-015-... 2 12/02/2010 Zimmer Inc.
Zimmer, NexGen Complete Knee Solution LPS Flex Gender Femoral Component, Size E Right, sterile, REF ... 2 12/02/2010 Zimmer Inc.
Zimmer, NexGen Complete Knee Solution LPS Femoral Component, Size F Left, sterile, REF 00-5996-016-0... 2 12/02/2010 Zimmer Inc.
Zimmer, NexGen Complete Knee Solution LPS Femoral Component, Size G Right, sterile, REF 00-5996-017-... 2 12/02/2010 Zimmer Inc.
Zimmer, NexGen Complete Knee Solution LPS Femoral Component, Size G Left, sterile, REF 00-5996-017-0... 2 12/02/2010 Zimmer Inc.
Zimmer, NexGen Complete Knee Solution LPS Femoral Component, Size F Right, sterile, REF 00-5996-016-... 2 12/02/2010 Zimmer Inc.
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