Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K030265 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Product 22 consists of all product under product code: JDI and same usage: Item no: 811400218 C... | 2 | 03/12/2016 | Zimmer Manufacturing B.V. |
CPT 12/14 COCR prosthesis, hip, semi-constrained, metal/polymer, porous uncemented various sizes ... | 2 | 02/22/2016 | Zimmer Biomet, Inc. |
CPT 12/14 COCR (various sizes) | 2 | 02/20/2014 | Zimmer, Inc. |
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