Medical Device Recalls
-
|
31 to 32 of 32 Results
510(K) Number: K181122 |
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and def... | 1 | 09/20/2024 | Datascope Corp. |
| CARDIOSAVE RESCUE INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and def... | 1 | 09/20/2024 | Datascope Corp. |
-







