Medical Device Recalls
-
21 to 21 of 21 Results
510(K) Number: K052013 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Achieva 1.5T | 2 | 11/21/2023 | Philips North America Llc |
-