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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 19 Results
510(K) Number: K960279
 
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LCCK FEM IMPLANT SZ C-L LCCK FEM IMPLANT SZ C-R LCCK FEM IMPLANT SZ D-R LCCK FEM IMPLANT SZ E-L ... 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 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 IMPLANT SZ H-R This device is indicated for patients with severe knee pain and disability 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.
Product 48 consists of all product under product code: JWH and same usage: Item no: 597206526 NE... 2 03/12/2016 Zimmer Manufacturing B.V.
NexGen Knee LPS Porous FEM NexGen Knee LPS Option FEM NexGen Knee Lock FEM prosthesis, knee, pate... 2 02/22/2016 Zimmer Biomet, Inc.
NexGen Augment; 5mm Distal Femoral Augment;Part number 00-5990-036-10. Intended to be used in tot... 2 05/01/2015 Zimmer, Inc.
MODULAR CUP NEUTRAL LINER MODULAR CUP 10 DEGREE LIN MODULAR CUP 20 DEGREE LIN MODULAR CUP 7MM OFF... 2 02/20/2014 Zimmer, Inc.
NexGen Complete Knee Solution Stemmed tibial broach impactor, Catalog # 00-5977-011-00, Zimmer Inc.,... 2 12/13/2010 Zimmer Inc.
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