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U.S. Department of Health and Human Services

Class 2 Device Recall SENSAR

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 Class 2 Device Recall SENSARsee related information
Date Initiated by FirmAugust 26, 2016
Date PostedSeptember 21, 2016
Recall Status1 Terminated 3 on December 23, 2016
Recall NumberZ-2855-2016
Recall Event ID 75051
PMA NumberP980040 
Product Classification intraocular lens - Product Code HQL
ProductSENSAR Foldable IOL with OptiEdge Design, Model No. AR40e The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed in the capsular bag.
Code Information Serial No. 5626941507 5626961507 5626981507 5627001507 2003061505 2004131506 2015871503 3848581509 5626621507 5626641507 5626651507 5626661507 5626671507 5626681507 5626691507 5626701507 5626711507 5626721507 5626731507 5626741507 5626751507 5626761507 5626771507 5626791507 5626801507 5626811507 5626821507 5626831507 5626841507 5626851507 5626861507 5626871507 5626881507 5626891507 5626901507 5626911507 5626921507 5626931507 5626951507 5626971507 5627011507 5627021507 5627031507 5627041507 5627051507 5627061507 5627071507 5627081507 5627091507 5627101507 5627111507 5627121507 5627131507 5627141507 5627151507 5627161507 5627171507 5627181507 5627191507 5627201507 5627211507 5627221507 
Recalling Firm/
Manufacturer		 Abbott Medical Optics Inc. (AMO)
1700 E Saint Andrew Pl
Santa Ana CA 92705-4933
For Additional Information Contact
714-247-8200
Manufacturer Reason
for Recall		Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they were not being checked prior to release and this may result in the release of mislabeled IOLs.
FDA Determined
Cause 2		Process control
ActionAbbott Medical Optics, Inc. sent an Urgent Field Safety Notice to all affected customers to inform them that Abbott Medical Optics (AMO) is recalling 737 IOLs due to detection of an inspection equipment malfunction that resulted in a total of 737 distributed lenses not being fully checked prior to release. The letter informs customers that this malfunction may result in the release of mislabeled IOLs. The letter informs the customers of the actions to be taken. Customers are instructed to complete Customer Reply Form and fax it to AMO Quality Assurance at 714-247-4510 or email to RegCompliOne@abbott.com. Customers with any questions related to the IOL return process are instructed to contact an AMO Customer Service Representative at 877-266-4543. Customers with product complaints or adverse events are instructed to inform AMO by calling 877-266-4543.
Quantity in Commerce84 units
DistributionWorldwide Distribution - US nationwide, PR, and Internationally to Canada, Latin America, Europe, Africa, Middle East, and Asia Pacific.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
PMA DatabasePMAs with Product Code = HQL
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