Medical Device Recalls
-
|
1 result found
510(K) Number: K122180 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Olympus High-Flow Insufflation Unit, Model UHI-4. For laparoscopic surgery. | 1 | 10/18/2023 | Olympus Corporation of the Americas |
-







