Medical Device Recalls
-
1 result found
510(K) Number: K854631 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
VERIFY® Dual Species Self-Contained Biological Indicator, Distributed by STERIS Corporation, Mentor,... | 2 | 12/28/2013 | Steris Corporation |
-