Medical Device Recalls
-
21 to 21 of 21 Results
510(K) Number: K031538 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Boston Scientific EndoVive 20F (6.7 mm) Safety PEG Kit, Push Method for use with pre-filled lidocain... | 2 | 01/28/2009 | Boston Scientific Corp |
-