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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
PMA Number: P930014
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Product Description
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FDA Recall
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Acrysof, IQ IOL w/UltraSert System, AcrySof IQ ASPHERIC IOL, 20.5 D, SP ACRYLIC FOLDABLE LENS, w/Ult... 2 06/05/2020 Alcon Research LLC
Alcon AcrySof IQ IOL with ULTRASERT Delivery System Product Usage: The Alcon AcrySof IQ Intraocu... 2 09/01/2016 Alcon Research, Ltd.
AcrySof® Intraocular Lens 2 02/15/2007 Alcon Laboratories, Inc
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