Medical Device Recalls
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1 to 2 of 2 Results
Related Medical Device Recalls |
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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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| Z-0131-2014 - GENESIS(R) II, NON-POROUS TIBIAL BASE, SIZE 6, RIGHT, QTY: (1), REF 71420188. Product Usage: orthopaedic | 2 | 11/01/2013 |
FEI # 1020279 Smith & Nephew Inc |
| Z-0130-2014 - GENESIS(R) II, NON-POROUS TIBIAL BASE, SIZE 5, LEFT, QTY: (1), REF 71420168. Product Usage: orthopaedic | 2 | 11/01/2013 |
FEI # 1020279 Smith & Nephew Inc |
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