Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K960278 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Product 11 consists of all product under product code JDI , and same usage: Item no: 902602500 6... | 2 | 03/12/2016 |
FEI # 1000132037 Zimmer Manufacturing B.V. |
| Product 64 consists of all product under product code: JDI and same usage: Item no: 902605101 UNI... | 2 | 03/12/2016 |
FEI # 1000132037 Zimmer Manufacturing B.V. |
| Endo & Unipolar Femoral Heads: ENDO FEMORAL HEAD 43MM DIA, ENDO FEMORAL HEAD 53MM DIA, ENDO FEMORAL... | 2 | 08/26/2014 |
FEI # 1000220733 Zimmer, Inc. |
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