Medical Device Recalls
-
|
1 to 6 of 6 Results
510(K) Number: K041281 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| LINEAR 7.5Fr.IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation t... | 2 | 07/21/2023 |
FEI # 1000222374 Datascope Corp. |
| LINEAR 7.5Fr. 40cc IAB with Accessories (APA), Model No. 0684-00-0480-02. intra-aortic balloon cath... | 2 | 10/24/2022 |
FEI # 1000222374 Datascope Corporation |
| Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 40cc IAB Kit P/N: 0684-00-0480-01, 0684... | 2 | 08/21/2020 |
FEI # 1000222374 Datascope Corporation |
| Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 25cc IAB Kit P/N: 0684-00-0478-01, 068... | 2 | 08/21/2020 |
FEI # 1000222374 Datascope Corporation |
| Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 34cc IAB Kit P/N: 0684-00-0479-01, 0684-... | 2 | 08/21/2020 |
FEI # 1000222374 Datascope Corporation |
| LINEAR 7.5 FR. 40cc IAB Catheter Maquet Getinge Group | 3 | 09/03/2014 |
FEI # 1000222374 Datascope Corporation |
-







