Medical Device Recalls
-
|
1 result found
510(K) Number: K132638 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Dimension Creatinine Flex reagent cartridge. Material Number: 10872079. | 2 | 04/28/2026 |
FEI # 2517506 Siemens Healthcare Diagnostics, Inc. |
-







