Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K190057 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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EMPOWR Acetabular System, Liner, 10® Hooded, HXe+, 40H, REF: 942-01-40H | 2 | 10/12/2023 | Encore Medical, LP |
EMPOWR Acetabular System, Liner, 10 deg Hooded, HXe+ 40H, REF: 942-01-40H. Orthopedic implant compon... | 2 | 10/21/2022 | Encore Medical, LP |
EMPOWR Acetabular System *** EMPOWR Acetabular Cup, Cluster Hole, 54G *** Size 54G 54 mm Dia./Clust... | 2 | 10/20/2020 | Encore Medical, LP |
EMPOWR Acetabular System, Non-Sterile, Model Numbers 803-15-023 803-15-026 803-15-027 803-15-02... | 2 | 05/08/2020 | Encore Medical, LP |
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