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-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. |
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 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 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. |
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