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U.S. Department of Health and Human Services

Class 2 Device Recall TECNIS Symfony, Extended Range of Vision

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  Class 2 Device Recall TECNIS Symfony, Extended Range of Vision see related information
Date Initiated by Firm July 06, 2023
Date Posted August 03, 2023
Recall Status1 Open3, Classified
Recall Number Z-2288-2023
Recall Event ID 92666
PMA Number P980040S065 
Product Classification Extended depth of focus intraocular lens - Product Code POE
Product TECNIS Symfony, Extended Range of Vision IOL, REF: ZXR00, STERILE.EO, Rx Only
Code Information UDI-DI: 5050474579163/ Serial Numbers: 8210142244, 8210152244, 8210162244, 8210172244, 8210182244, 8210192244, 8210202244, 8210212244, 8210222244, 8210232244, 8210242244, 8210252244, 8210262244, 8210272244, 8210282244, 8210292244, 8210302244, 8210312244, 8210322244, 8210332244, 8210342244, 8210352244, 8210362244, 8210372244, 8210382244, 8210392244, 8210402244, 8210412244, 8210422244, 8210432244, 8210442244, 8210452244, 8210462244, 8210472244, 8210482244, 8210492244, 8210502244, 8210512244, 8210522244, 8210532244, 8210542244, 8210552244.
Recalling Firm/
Johnson & Johnson Surgical Vision, Inc.
31 Technology Dr Ste 200
Irvine CA 92618-2302
Manufacturer Reason
for Recall
Their is a potential that intraocular lenses (IOLs) were manufactured with unintended toric fiducial marks.
FDA Determined
Cause 2
Under Investigation by firm
Action On June 07, 20223, Johnson & Johnson Vison issued an "Urgent: Medical Device Recall" notice to affected consignees. Consignees were asked to take the following actions: 1. Identify if any of your inventory contains TECNIS¿ IOLs from the list on pages 5-6 (see page 4 for label examples). 2. Remove all affected TECNIS¿ IOLs from your inventory. No other TECNIS¿ IOLs are affected by this recall. 3. Complete the attached Customer Reply Form (on page 3). We require this information for reconciliation purposes with regulatory agencies, even if you have no inventory. 4. Follow the specific instructions included in the letter "If you have product to be returned" or "If you do not have product to be returned" 5. Share this notice with anyone within your organization that needs to be informed and to any organization where the potentially affected products have been transferred. 6. If you have product complaints or adverse events to report regarding the use of the affected TECNIS¿ IOLs, please inform Johnson & Johnson Vision. If you do report a complaint, please provide the TECNIS¿ IOL serial number and, if a patient was involved, the date of surgery, a description of the event and patient outcome. 7. In addition, you may report any adverse events experienced or quality issues with the use of the TECNIS¿ IOLs to the FDA's MedWatch Adverse Event Reporting program by phone at 1-800-332-1088, by fax at 1-800-332-0178, by mail at MedWatch, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch Web site at www.fda.gov/medwatch/report.htm.
Quantity in Commerce 42
Distribution International distribution to the countries of China, India, Korea.
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 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
PMA Database PMAs with Product Code = POE and Original Applicant = Johnson & Johnson Surgical Vision, Inc.