Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K122628 |
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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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Sensation Plus 7.5Fr. 40cc Intra-Aortic Balloon Catheter with accessories, Part Number 0684-00-0568-... | 2 | 07/12/2019 | Datascope Corporation |
SENSATION PLUS 7.5Fr IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pul... | 2 | 07/21/2023 | Datascope Corp. |
Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation Plus 7.5 Fr 40cc IAB Kit P/N: 0684-00-0568-... | 2 | 08/21/2020 | Datascope Corporation |
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