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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 18 Results
510(K) Number: K953510
 
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Product Description
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FDA Recall
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Foundation® Hip System Bipolar Modular, Size 40mm OD; Cat. #412-01-040; Sterile; assembly required b... 2 11/07/2007 Encore Medical, Lp
Foundation® Hip System Bipolar Modular, Size 60mm OD; Cat. #412-01-060; Sterile; assembly required b... 2 11/07/2007 Encore Medical, Lp
Foundation® Hip System Bipolar Modular, Size 42mm OD; Cat. #412-01-042; Sterile; assembly required b... 2 11/07/2007 Encore Medical, Lp
Foundation® Hip System Bipolar Modular, Size 43mm OD; Cat. #412-01-043; Sterile; assembly required b... 2 11/07/2007 Encore Medical, Lp
Foundation® Hip System Bipolar Modular, Size 44mm OD; Cat. #412-01-044; Sterile; assembly required b... 2 11/07/2007 Encore Medical, Lp
Foundation® Hip System Bipolar Modular, Size 45mm OD; Cat. #412-01-045; Sterile; assembly required b... 2 11/07/2007 Encore Medical, Lp
Foundation® Hip System Bipolar Modular, Size 46mm OD; Cat. #412-01-046; Sterile; assembly required b... 2 11/07/2007 Encore Medical, Lp
Foundation® Hip System Bipolar Modular, Size 47mm OD; Cat. #412-01-047; Sterile; assembly required b... 2 11/07/2007 Encore Medical, Lp
Foundation® Hip System Bipolar Modular, Size 48mm OD; Cat. #412-01-048; Sterile; assembly required b... 2 11/07/2007 Encore Medical, Lp
Foundation® Hip System Bipolar Modular, Size 49mm OD; Cat. #412-01-049; Sterile; assembly required b... 2 11/07/2007 Encore Medical, Lp
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