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U.S. Department of Health and Human Services

Medical Device Recalls

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1 result found
510(K) Number: K033919
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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O®Optix® (lotrafilcon B) Soft Contact Lenses, Rx only, Ciba Vision. The product is distributed in 3 ... 2 02/15/2007 Ciba Vision Corporation
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