Medical Device Recalls
-
|
1 result found
510(K) Number: K251327 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| XERF EFFECTOR 60. Electrosurgical unit. | 2 | 10/14/2025 | Lutronic Corporation |
-







