Medical Device Recalls
-
|
1 result found
510(K) Number: K831087 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Low Volume Extension Set, 72' w/Clamp FLL/MLL APV=1.3ml, STERILE, AND FLUID PATH NONPYROGENIC UNLESS... | 2 | 06/08/2015 |
FEI # 1526863 Smiths Medical Asd Inc |
-







