Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K142281 |
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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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| Various fixation systems and accessories, Item Nos. 00224000916 00224000918 00224000920 002240009... | 2 | 11/07/2019 |
FEI # 1000220733 Zimmer Biomet, Inc. |
| FEM IM NAIL 14MMDX30CM LEFT, FEM IM NAIL 14MMDX30CM RIGHT FEM IM NAIL 13MMDX32CM LEFT FEM IM NAIL ... | 2 | 06/15/2017 |
FEI # 1000220733 Zimmer Biomet, Inc. |
| R-F IM NAIL 10MMDX48CM LG, 11MMDX42CM, 11MMDX44CM, 11MMDX46CM LG, 11MMDX48CM LG, 12MMDX46CM LG, 12... | 2 | 06/15/2017 |
FEI # 1000220733 Zimmer Biomet, Inc. |
| M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw, 3.5 mm Hex Head, 45 mm Length 002253045... | 2 | 05/16/2016 |
FEI # 1000132037 Zimmer Manufacturing B.V. |
| Product 38 consists of all product under product code: HSB and same usage: Item no: 225303255 IN... | 2 | 03/12/2016 |
FEI # 1000132037 Zimmer Manufacturing B.V. |
| Product 43 consists of all product under product code: HSB and same usage: Item no: 224001016 M/... | 2 | 03/12/2016 |
FEI # 1000132037 Zimmer Manufacturing B.V. |
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