Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K945484 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Integra Disposable, Convenience Kit Single Shot Epidural Tray Reorder Number 340269 Rx Only Pro... | 2 | 12/17/2013 |
FEI # 1000138491 Integra LifeSciences Corp. d.b.a. Integra Pain Management |
| Single Shot Epidural Trays, Sterile, Integra Pain Management, West Valley City, Utah 84119, each kit... | 3 | 07/05/2012 |
FEI # 1000138491 Integra LifeSciences Corp. d.b.a. Integra Pain Management |
-







