Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K203557 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID2... | 2 | 07/21/2025 | Encore Medical, LP |
| Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID2... | 2 | 07/21/2025 | Encore Medical, LP |
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