Medical Device Recalls
-
1 to 2 of 2 Results
Recall Date to: 09/21/2014 510(K) Number: K040049 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Reliance Endoscope Processing System (REPS), STERIS Corporation, 5960 Heisley Road, Mentor, OH 44060... | 2 | 09/20/2013 | Steris Corporation |
Steris Reliance EPS Endoscope Processing System , manufactured by Corporation STERIS Canada, Quebec,... | 3 | 12/28/2010 | Steris Corporation |
-