Medical Device Recalls
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1 result found
Recall Number: Z-2545-2017 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Best Practice Kit, Item Numbers: 00Z2064, 00Z2150, 00Z2190, 00Z2192, 00Z2211, 00Z2212, 00Z2216, 00Z2... | 2 | 06/14/2017 |
FEI # 1219930 Medtronic |
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