Medical Device Recalls
-
|
1 result found
510(K) Number: K141385 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| RAPIDSORB IPS Battery Pack, Sterile-Intended for use in non-load bearing fracture repair and reconst... | 2 | 03/01/2024 |
FEI # 3008812560 Synthes (USA) Products LLC |
-







