Medical Device Recalls
-
|
1 result found
510(K) Number: K170316 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Alinity ci-series System Control Module (SCM), REF: 03R70-01, 03R70-20 | 2 | 12/18/2025 |
FEI # 3016438761 Abbott Laboratories |
-







