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U.S. Department of Health and Human Services

Class 2 Device Recall TECNIS

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  Class 2 Device Recall TECNIS see related information
Date Initiated by Firm August 26, 2016
Date Posted September 21, 2016
Recall Status1 Terminated 3 on December 23, 2016
Recall Number Z-2861-2016
Recall Event ID 75051
PMA Number P980040 
Product Classification intraocular lens - Product Code HQL
Product TECNIS 1-Piece IOL with the TECNIS iTec Preloaded Delivery System, Model No. PCB00
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. 7138841403 2648831412 2648971412 2649011412 2649071412 2649101412 2649181412 2649221412 2649241412 2649261412 2649281412 2649301412 7138301403 7138311403 7138321403 7138331403 7138341403 7138351403 7138361403 7138371403 7138381403 7138391403 7138401403 7138411403 7138431403 7138441403 7138451403 7138461403 7138471403 7138481403 7138491403 7138501403 7138511403 7138521403 7138531403 7138541403 7138551403 7138561403 7138571403 7138581403 7138591403 7138601403 7138611403 7138621403 7138631403 7138641403 7138651403 7138661403 7138671403 7138681403 7138691403 7138701403 7138711403 7138721403 7138731403 7138741403 7138751403 7138761403 7138771403 7138781403 7138791403 7138801403 7138811403 7138821403 7138831403 7138851403 7138881403 7138891403 7138901403 7138911403 7138921403 7138941403 7138951403 7138961403 7138971403 7138981403 7138991403 7139001403 7139011403 7139021403 7139031403 7139041403 7139051403 7139061403 7139071403 7139081403 7139091403 7139101403 7139111403 7139121403 7139131403 7139141403 2648751412 2648761412 2648771412 2648781412 2648791412 2648801412 2648811412 2648821412 2648841412 2648851412 2648861412 2648871412 2648881412 2648891412 2648901412 2648911412 2648921412 2648931412 2648941412 2648951412 2648961412 2648981412 2648991412 2649001412 2649021412 2649031412 2649041412 2649061412 2649081412 2649091412 2649111412 2649121412 2649131412 2649141412 2649151412 2649161412 2649171412 2649191412 2649201412 2649211412 2649231412 2649251412 2649271412 2649291412 2649311412 2397761605 2397981605 3125171501 3125181501 7731731310 7731741310 7731751310 7731761310 7731771310 7731781310 7731791310 7731801310 7731811310 7731821310 7731831310 7731841310 7731851310 7731861310 7731871310 7731881310 7731891310 7731901310 7731911310 7731921310 7731931310 7731941310 7731951310 7731961310 7731971310 7731981310 7731991310 7732001310 7732011310 7732021310 7732031310 7732041310 7732051310 7732061310 7732071310 7732081310 7732091310 7732101310 7732121310 7732131310 7732141310 7732151310 7732161310 7732181310 7732191310 7732201310 7732211310 7732221310 7732231310 7732241310 7732251310 7732261310 7732271310 7732281310 7732291310 7732301310 7732311310 7732321310 7732331310 7732341310 7732361310 7732371310 7732391310 7732401310 7732411310 7732421310 7732431310 7732441310 7732451310 7732461310 7732471310 7732481310 7732491310 7732501310 7732511310 7732521310 
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
Action Abbott 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 Commerce 217 units
Distribution Worldwide Distribution - US nationwide, PR, and Internationally to Canada, Latin America, Europe, Africa, Middle East, and Asia Pacific.
Total Product Life Cycle TPLC 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 Database PMAs with Product Code = HQL and Original Applicant = Johnson & Johnson Surgical Vision, Inc.
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