Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K020802 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Equate Muti-Purpose Solution, For Soft Contact Lenses, Sterile, 12 Fl oz. (355 mL), Distributed by W... | 3 | 08/19/2011 |
FEI # 1317628 Bausch & Lomb Inc |
| Contact lens solution. The product is distributed under the following trade names: Bausch & Lomb Re... | 2 | 04/04/2007 |
FEI # 1317628 Bausch & Lomb Inc |
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