Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K983836 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Bausch & Lomb Boston® Conditioning Solution, Original Formula, Bausch & Lomb Incorporated, Rochester... | 2 | 12/22/2009 | Bausch & Lomb Inc |
Bausch & Lomb, Boston® Conditioning Solution, Original Formula, For Rigid Gas Permeable Contact Lens... | 2 | 08/13/2009 | Bausch & Lomb Inc |
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