Medical Device Recalls
-
|
1 result found
510(K) Number: K233983 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Swan-Ganz Pacing Catheter, Models: D200F7; | 2 | 05/15/2026 |
FEI # 3032916632 Becton, Dickinson and Company |
-







