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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-2154-2015
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Bausch & Lomb SoFlex SE Foldable intraocular Lens Product Usage: The SofPort/SoFlex IOLs are int... 2 07/20/2015 FEI # 1119279
Bausch & Lomb Surgical, Inc.
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