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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 24 Results
510(K) Number: K031061
 
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NexGen CR-Flex Femoral Component, Size E and Size E Minus (E-). Component of the NexGen CR-Flex Poro... 2 04/22/2024 Zimmer, Inc.
LPS PRECOAT FEM SIZE D-RT LPS PRECOAT FEM SIZE E-RT LPS POROUS FEM SIZE F-RT This device is ind... 2 03/14/2018 Zimmer Biomet, Inc.
CR POR FEM HATCP SIZE E/L SIZE F/L Knee Prosthesis 2 03/14/2018 Zimmer Biomet, Inc.
CR-FLEX POR FEM F-L CR-FLEX POR FEM F-R MINUS CR-FLEX POR FEM G-L This device is indicated for ... 2 03/14/2018 Zimmer Biomet, Inc.
CR PRECOAT FEM COMP SIZE BMR CR PRECOAT FEM COMP SIZE C/R CR PRECOAT FEM COMP SIZE D/R CR PRECOAT... 2 03/14/2018 Zimmer Biomet, Inc.
LPS PRECOAT SRF HDN FEM SZ D-L LPS PRECOAT SRF HDN FEM SZ D-R LPS PRECOAT SRF HDN FEM SZ E-L LPS ... 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.
Nextgen Complete Knee Solution Replacement Jaw for Use with Femoral and Provisional Impactor/Extract... 2 07/27/2012 Zimmer Inc.
Nextgen Complete Knee Solution Femoral and Provisional Impactor/ Extractor, REF 00-5901-026-00, Non... 2 07/27/2012 Zimmer Inc.
NEXGEN COMPLETE KNEE SOLUTION FEMORAL AND PROVISIONAL IMPACTOR/EXTRACTOR, NONSTERILE, REF 00-5901-0... 2 05/10/2011 Zimmer Inc.
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