Medical Device Recalls
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1 to 3 of 3 Results
PMA Number: P930014 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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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