Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K063331 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Bausch & Lomb Stellaris 1.8mm Micro Incision AFS Phaco Pack with MICS Angled Needle, Model BL5123A, ... | 2 | 05/28/2010 | Bausch & Lomb Inc |
Bausch & Lomb Stellaris Vision Enhancement System. | 2 | 05/26/2010 | Bausch & Lomb Inc |
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