Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K191325 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| EMPOWR Partial Knee Peg Drill; Model: 800-06-008. | 2 | 11/20/2020 | Encore Medical, LP |
| EMPOWR Partial Knee Peg Drill Guide; Model: 800-06-007. | 2 | 11/20/2020 | Encore Medical, LP |
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