Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K002099 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Neulook Deluxe is packaged in a pink soft plastic box with white, black, and rainbow printing that r... | 2 | 01/11/2012 |
FEI # 3009014092 Eyezone |
| Neulook Fancy FX is packaged in a small glass bottle with a orange, white, and yellow affixed label ... | 2 | 01/11/2012 |
FEI # 3009014092 Eyezone |
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