Medical Device Recalls
-
1 result found
510(K) Number: K033941 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Bausch & Lomb Millennium Advanced Flow System Phaco Pack, Model CX5310, 6 packs/box, RX, Sterile. T... | 2 | 05/28/2010 | Bausch & Lomb Inc |
-