Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K032367 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Zimmer ITST Intertrochanteric/subtrochanteric fixation taper reamer - Asia, nonsterile; REF 2258-50-... | 2 | 08/04/2009 | Zimmer Inc. |
Zimmer ITST Intertrochanteric/subtrochanteric fixation tapered reamer, nonsterile; REF 2258-50-00. | 2 | 08/04/2009 | Zimmer Inc. |
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