MAUDE Adverse Event Report: RXSIGHT, INC. LIGHT ADJUSTABLE LENS (LAL)

Model Number	60005
Medical Device Problem Code	Optical Problem (3001)
Health Effect - Clinical Code	Visual Impairment (2138)
Date of Event	05/25/2021
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Site reported that the light adjustable lens in the patient's right eye was explanted as the patient was experiencing double vision.Rxsight's first awareness of the event was (b)(6) 2021.Device history record for the lens was reviewed.No issues were noted.The explanted lens has been received and is pending evaluation results.
Event or Problem Description
Site reported that the light adjustable lens in the patient's right eye was explanted as the patient was experiencing double vision.Rxsight's first awareness of the event was (b)(6) 2021.
Event or Problem Description
Site reported that the light adjustable lens in the patient's right eye was explanted as the patient was experiencing double vision.Rxsight's first awareness of the event was 6/18/2021.
Additional Manufacturer Narrative
Site reported that the light adjustable lens in the patient's right eye was explanted as the patient was experiencing double vision.Rxsight's first awareness of the event was 6/18/2021.The returned lens was visually inspected and optically tested.A zone was noted near the center of the lens optic.The presence of a zone indicates the lens was exposed to ambient uv light prior to lock in.

• Brand Name: LIGHT ADJUSTABLE LENS (LAL)
• Common Device Name: LIGHT ADJUSTABLE LENS (LAL)
• Manufacturer (Section D): RXSIGHT, INC.; 100 columbia; aliso viejo CA 92656
• MDR Report Key: 12182358
• Report Number: 3012712027-2021-00032
• Device Sequence Number: 2825408
• Product Code: PZK
• UDI-Device Identifier: 00818806020210
• UDI-Public: 010081880602021017220930
• Combination Product (Y/N): N
• Initial Reporter State: NE
• Initial Reporter Country: US
• PMA/510(K) Number: P160055
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2020
• Device Explanted Year: 2021
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: health professional,user faci
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 07/16/2021

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: 09/30/2022
• Device Model Number: 60005
• Device Catalogue Number: 60005
• Device Lot Number: L02-001384
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 06/28/2021
• Initial Date Received by Manufacturer: 06/18/2021
• Supplement Date Received by Manufacturer: 06/18/2021
• Initial Report FDA Received Date: 07/16/2021
• Supplement Report FDA Received Date: 08/26/2021
• 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: Required Intervention