Medical Device Recalls
-
|
1 result found
Related Medical Device Recalls |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Z-2317-2018 - Single Chamber Temporary External Pacemaker, Model 53401 | 2 | 06/29/2018 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
-







