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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K190057
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Product Description
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FDA Recall
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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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