Medical Device Recalls
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21 to 23 of 23 Results
510(K) Number: K955848 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ORTHOFIX Catalogue Number: ref: 99-92503, PREFIX II DIAPHYSEAL COMPLETE KIT STERILE LONG SCREWS, RX... | 2 | 11/14/2019 | Orthofix Srl |
Orthofix US XCaliber Meta-Diaphyseal Complete Kit, Sterile. 99-91600, manufactured by Orthofix SRL, ... | 2 | 04/28/2010 | Orthofix Srl |
Orthofix US XCaliber Ankle Complete Kit, Sterile, 99-91647. manufactured by Orthofix SRL, Via delle ... | 2 | 04/28/2010 | Orthofix Srl |
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