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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 15 Results
PMA Number: P060037
 
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Product Description
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FDA Recall
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Zimmer NexGen Complete Knee Solution Legacy Knee- Posterior Stabilized LPS-FLEX Femoral Component Op... 2 06/25/2009 Zimmer Inc.
Zimmer NexGen Complete Knee Solution Legacy Knee- Posterior Stabilized LPS-FLEX Femoral Component Op... 2 06/25/2009 Zimmer Inc.
Zimmer NexGen Complete Knee Solution Legacy Knee- Posterior Stabilized LPS Femoral Component Option ... 2 06/25/2009 Zimmer Inc.
Zimmer NexGen Complete Knee Solution Legacy Knee - Posterior Stabilized LPS-Flex Femoral Component P... 2 06/25/2009 Zimmer Inc.
NexGen CR-Flex Mobile Bearing Tibial Component 9 (Not distributed in the United States) 2 10/25/2013 Zimmer, Inc.
NexGen LPS Flex Option Femoral NexGen LPS Flex Precoat Femoral prosthesis, knee, patellofemorotibi... 2 02/22/2016 Zimmer Biomet, Inc.
NexGen LPS Femoral Component, Left and Right, Size G Replaces the femoral condyle of the knee joi... 2 02/21/2018 ZIMMER ORTHOPEDIC MFG LTD
LPS OPTION FEMORAL C-L LPS OPTION FEMORAL C-R LPS OPTION FEMORAL D-L LPS OPTION FEMORAL D-R LPS ... 2 03/14/2018 Zimmer Biomet, Inc.
LPS FEM COMP SZ B-L LPS FEM COMP SZ B-R LPS FEM COMP SZ C-L LPS FEM COMP SZ C-R LPS FEM COMP SZ ... 2 03/14/2018 Zimmer Biomet, Inc.
LPS POROUS FEM IMPLANT SZ G-L LPS PRECOAT FEM IMPLANT SZ G-L This device is indicated for patien... 2 03/14/2018 Zimmer Biomet, Inc.
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