Medical Device Recalls
-
|
1 result found
510(K) Number: K791871 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Pilling Wecksorb Cylindrical Sponges | 2 | 12/28/2022 | TELEFLEX LLC |
-







