MAUDE Adverse Event Report: AMO PUERTO RICO MFG. INC. TECNIS IOL; LENS, MULTIFOCAL INTRAOCULAR

Model Number	DFW225
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Visual Disturbances (2140)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Additional information: patient weight and ethnicity: unknown/asked but unavailable.Date of event: unknown as information was not provided, the best estimate date is within days of first surgery, (b)(6) 2022.Date explanted: not applicable as the iol remains implanted.It was indicated that the iol is not being returned for evaluation as it remains implanted in the patient¿s ocular sinister (left eye).Therefore, a visual analysis of the complaint device cannot be completed.A review of the device history record and historical data analysis for this device will be performed.Upon completion of the review, if there is any further relevant information a supplemental medwatch report will be filed.Attempts were made to contact the customer account requesting additional information regarding complaint however, to date no response has been received.All pertinent information available to johnson & johnson surgical vision, inc.Has been submitted.
Event or Problem Description
It was reported the dfw225 intraocular lens (iol) was implanted into the patient¿s ocular sinister (left eye).Patient reports complaints of inability to drive at night within days of first surgery.There was no patient injury.Iol explant is scheduled for (b)(6) 2023 and the planned replacement lens is a non-johnson & johnson surgical vision 16.0 diopter lens.No further information is available.
Additional Manufacturer Narrative
Correction: device was returned thus indicating the iol was explanted.The following fields were updated accordingly: section d-6b date explanted: unknown, information not provided.Previously reported in the initial report as n/a as device remains implanted.Section h-6 health effect - impact code: updated to 4629 - device revision or replacement, previously reported in the initial report as 2199 - no health consequences or impact.Additional information: section d-9: device available for evaluation: yes.Section d-9: device date returned to manufacturer: 14-aug-2023.Section h-3: device evaluated by manufacturer: yes.Device evaluation: one lens was received inside of a specimen cup marked with two sn's.Sn: (b)(6) and sn: (b)(6).Since it cannot be determined which investigation the lens belongs to, it will be evaluated in both investigations.Visual inspection under magnification revealed that the complaint lens was received cut in half.The lens was cleaned and, no issues that could cause or contribute to the complaint issue.Based on the return condition of the lens, no further product evaluation could be performed.The complaint issue was not confirmed.The other observed issues during the product evaluation could not be confirmed to be related to a manufacturing or design issue.Conclusion: based on the complaint investigation results, the product was released within specifications.The complaint issue reported could not be confirmed and no product deficiency or product malfunction could be identified.All pertinent information available to johnson & johnson surgical vision, inc.Has been submitted.

• Brand Name: TECNIS IOL
• Common Device Name: LENS, MULTIFOCAL INTRAOCULAR
• Manufacturer (Section D): AMO PUERTO RICO MFG. INC.; road 402 north, anasco ind. pk; anasco PR 00610
• Manufacturer Contact: somyata nagpal ; 31 technology drive; irvine, CA 92618 ; 7142478552
• MDR Report Key: 16343934
• Report Number: 3012236936-2023-00212
• Device Sequence Number: 12341856
• Product Code: MFK
• UDI-Device Identifier: 05050474751781
• UDI-Public: (01)05050474751781(17)241108
• Combination Product (Y/N): N
• Initial Reporter State: OR
• Initial Reporter Country: US
• PMA/510(K) Number: P980040
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2022
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 10/09/2023

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: 11/08/2024
• Device Model Number: DFW225
• Device Catalogue Number: DFW225U165
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/18/2023
• Supplement Date Received by Manufacturer: 09/25/2023
• Initial Report FDA Received Date: 02/09/2023
• Supplement Report FDA Received Date: 10/09/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 11/08/2021
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Female