MAUDE Adverse Event Report: ABBOTT MEDICAL OPTICS TECNIS 1 MULTIFOCAL; MULTIFOCAL IOLS

Model Number	ZMB00
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
The best estimate is 2015, about 2 years ago.Remains implanted in the eye.Device evaluation: the intraocular lens (iol) was not returned to the manufacturing site as the lens remain implanted and not being returned.Therefore, product testing could not be performed and the customer¿s reported complaint could not be verified.Manufacturing records review: the manufacturing records for the intraocular lens were reviewed.The product was manufactured and released according to specification.Labeling review: the directions for use (dfu) was reviewed.The dfu adequately provides instructions and precautions along with warnings for the proper use and handling of the device.As a result of the investigation there is no indication of a product quality deficiency and the reported issue could not be verified.All pertinent information available to abbott medical optics has been submitted.
Event or Problem Description
A patient called to report that a zmb00 13.0 diopter intraocular lens (iol) was implanted in her right eye on (b)(6) 2013.Patient also had another lens, same model implanted in her left eye, (b)(6) 2013.She reported that for about 2 years she was pleased with the lenses; but for the last year, they are not as effective as in the beginning.She reported having to get her head closer and closer to the computer screen, and on the streets, she does not see the names of them as well as before.As patient had bilateral lens implants; a report will be filed for each eye.This report represents the patient''s right eye.

• Brand Name: TECNIS 1 MULTIFOCAL
• Common Device Name: MULTIFOCAL IOLS
• Manufacturer (Section D): ABBOTT MEDICAL OPTICS; santa ana CA
• MDR Report Key: 7204686
• Report Number: 2648035-2018-00147
• Device Sequence Number: 13747446
• Product Code: MFK
• UDI-Device Identifier: 05050474535480
• UDI-Public: (01)05050474535480(17)170201
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: P980040
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2013
• Reporter Type: Manufacturer
• Report Source: consumer
• Initial Reporter Occupation: Patient
• Type of Report: Initial
• Report Date (Section B): 01/18/2018

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: Physician
• Device Expiration Date: 02/01/2017
• Device Model Number: ZMB00
• Device Catalogue Number: ZMB00U0130
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/22/2017
• Initial Report FDA Received Date: 01/18/2018
• 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