Medical Device Recalls
-
21 to 22 of 22 Results
PMA Number: P010014 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Oxford Unicompartmental Knee Phase 3 Shim Size 3 Product Usage: Instruments for use with the Oxfor... | 2 | 02/22/2017 | Biomet U.K., Ltd. |
Oxford Unicompartmental Knee Phase 3 Tibial Impactor Product Usage: Instruments for use with the O... | 2 | 02/22/2017 | Biomet U.K., Ltd. |
-