Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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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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Z-1462-2023 - MAQUET CARDIOSAVE hybrid Intra-Aortic Balloon Pump, Model Number 0998-XX-0800-32 | 2 | 04/26/2023 | Datascope Corp. |
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