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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 83 Results
510(K) Number: K933785
 
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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 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.
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.
CR OPTION FEM COMP SIZE C/L CR OPTION FEM COMP SIZE C/R CR OPTION FEM COMP SIZE D/L CR OPTION FEM... 2 03/14/2018 Zimmer Biomet, Inc.
NexGen Offset Stem Extension, sizes 14mm and 17mm For use in total arthroplasty. 2 05/18/2017 Zimmer Biomet, Inc.
Product 49 consists of all product under product code: JWH and same usage: Item no: 597206529 NE... 2 03/12/2016 Zimmer Manufacturing B.V.
Product 53 consists of all product under: product code: JWH and same usage: Item no: 597002501... 2 03/12/2016 Zimmer Manufacturing B.V.
Product 61 consists of all product under product code: JWH and same usage: Item no: 598003712 STD... 2 03/12/2016 Zimmer Manufacturing B.V.
NexGen Knee CR Option Fem NexGen Knee CR Porous Fem NexGen Knee CR Precoat Fem NexGen Knee LPS Po... 2 02/22/2016 Zimmer Biomet, Inc.
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