MAUDE Adverse Event Report: JOHNSON & JOHNSON SURGICAL VISION, INC. TECNIS; TORIC IOLS

Model Number	ZCT225
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Corneal Edema (1791); Visual Impairment (2138); No Code Available (3191)
Date of Event	09/10/2019
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).All pertinent information available to johnson & johnson surgical vision, inc.Has been submitted.
Event or Problem Description
It was reported that the doctor implanted, in patient's left eye, a model zct525 intraocular lens based on the results taken from the lens calculations done (b)(6) 2019.The patient had a 3d (diopter) astigmatism correction requirement.Lens was placed.Reportedly, the patient had some corneal edema and was 20/400 post op.Doctor indicated a lens exchange may be necessary; however, patient does not want another surgery due to her other health conditions, reported to be a recent stroke.Further information was provided and indicates the doctor used the recommendation from the toric calculator completed (b)(6) 2019.It suggests a zct525 for correction of 3 d of cylinder so the zct525 was implanted.To assist the doctor, the account executive reran the numbers through the calculator and it recommended a model zct400.Patient will continue to be seen in follow up visits.Per the doctor, on line j of the calculator it recommended a model zct525 for implant in the patient's eye; however, at post op, patient was over corrected for astigmatism.Post op visit: (b)(6) 2019 - patient visual acuity 20/70 and no near vision.Further update from the doctor received (b)(6) 2019, reports the patient had her companion (right) eye implanted with a model zct225 (b)(6) 2019.Patient has anisometropia because of error of software for lens calculation for the left eye.Patient does not want any further surgery because of health reasons.Recent visit notes patient sees 20/50, zero close up, + 1.50 cylinder in the opposite direction but not clear vision.Patient is happy to wear glasses.The glasses correct the unexpected post op results.This report represents the right eye.A separate report is being filed for the left eye.No further information was provided.
Additional Manufacturer Narrative
Device evaluation: product evaluation was not performed as the lens was not returned; it remains.The complaint issue reported could not be verified and no product deficiency could be identified.Manufacturing records review: the manufacturing records for the device were reviewed.The product was manufactured and released according to specification.A search of complaints revealed that no similar complaints have been received for this production order.Based on the results of the investigation, no product deficiency was identified.All pertinent information available to johnson & johnson surgical vision, inc.Has been submitted.
Additional Manufacturer Narrative
This correction mdr is being submitted to address inaccurate information in section f on the xml version of the previous submission caused by a software glitch in the transmission process.The internal non-conformance numbers for this software issue are nr-(b)(4) and capa-010215.

• Brand Name: TECNIS
• Common Device Name: TORIC IOLS
• Manufacturer (Section D): JOHNSON & JOHNSON SURGICAL VISION, INC.; 1700 e st andrew place; santa ana CA 92705
• MDR Report Key: 9189135
• Report Number: 9614546-2019-00968
• Device Sequence Number: 16747498
• Product Code: HQL
• UDI-Device Identifier: 05050474552616
• UDI-Public: (01)05050474552616(17)220616
• Combination Product (Y/N): Y
• Initial Reporter State: CA
• Initial Reporter Country: US
• PMA/510(K) Number: P980040
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2019
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 11/09/2020
• Report Date (Section F): 01/01/2005

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Expiration Date: 06/18/2022
• Device Model Number: ZCT225
• Device Catalogue Number: ZCT225U140
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Date Report to Manufacturer: 01/10/2005
• Initial Date Received by Manufacturer: 09/17/2019
• Supplement Date Received by Manufacturer: 10/23/2019; 10/25/2020
• Initial Report FDA Received Date: 10/14/2019
• Supplement Report FDA Received Date: 10/24/2019; 11/10/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Age: 74 YR
• Date Report Sent to FDA: 01/01/2005