Medical Device Recalls
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1 result found
510(K) Number: K132216 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PeroxiClear Peroxide Solution, (3oz. and 12 oz., 12 oz. Twin Pack, 2x12 oz. Twin Pack for Target sto... | 2 | 11/21/2016 |
FEI # 1317628 Bausch & Lomb Inc Irb |
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