Medical Device Recalls
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1 result found
Recall Number: Z-3137-2024 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| CARDIOSAVE RESCUE INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and def... | 1 | 09/20/2024 |
FEI # 3001418283 Datascope Corp. |
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