Medical Device Recalls
-
|
1 result found
510(K) Number: K213363 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Carescape B450, Model no. 5805686 - shipped with potentially affected batteries or affected batterie... | 2 | 11/07/2025 |
FEI # 3002806783 GE Healthcare Finland Oy |
-







