Medical Device Recalls
-
|
1 result found
510(K) Number: K211125 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Novum IQ Syringe infusion system, Product Code 40800BAXUS | 1 | 11/09/2023 |
FEI # 1417572 Baxter Healthcare Corporation |
-







