Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-0535-2018 - Medtronic Custom Perfusion Systems, indicated for use in the extracorporeal circuit during cardiopulmonary bypass (CPB) surgical procedures. | 2 | 01/30/2018 |
FEI # 1000116158 Medtronic Perfusion Systems |
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