Medical Device Recalls
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11 to 15 of 15 Results
PMA Number: P060037 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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. |
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-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION FEMORAL C-R LPS-FLEX OPTI... | 2 | 03/14/2018 | Zimmer Biomet, Inc. |
NEXGEN LPS-FLEX PRECOAT FEMORAL SIZE E-LT This device is indicated for patients with severe knee ... | 2 | 03/14/2018 | Zimmer Biomet, Inc. |
NexGen LPS Flex Option Femoral NexGen LPS Flex Precoat Femoral prosthesis, knee, patellofemorotibi... | 2 | 02/22/2016 | Zimmer Biomet, Inc. |
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