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

Model Number	60005
Medical Device Problem Code	Optical Distortion (3000)
Health Effect - Clinical Code	Visual Disturbances (2140)
Date of Event	08/05/2021
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Site reported that the light adjustable lens was explanted from the patient's left eye due to dissatisfaction with glare.The patient's correctable vision was noted to be 20/15.Another lal was implanted during the exchange.Rxsight's first awareness of the issue was 8/5/2021.The device history record for the lens was reviewed.No issues were noted.The lens has not yet been received for evaluation.
Event or Problem Description
Site reported that the light adjustable lens was explanted from the patient's left eye due to dissatisfaction with glare.The patient's correctable vision was noted to be 20/15.Another lal was implanted during the exchange.Rxsight's first awareness of the issue was 8/5/2021.
Additional Manufacturer Narrative
Site reported that the light adjustable lens was explanted from the patient's eye due to dissatisfaction with glare.The patient's correctable vision was noted to be 20/15.Another lal was implanted during the exchange.Rxsight's first awareness of the issue was (b)(6) 2021.The explanted lens was returned in fragments.Visual inspection and optical testing found no issues with the returned lens.
Event or Problem Description
Site reported that the light adjustable lens was explanted from the patient's eye due to dissatisfaction with glare.The patient's correctable vision was noted to be 20/15.Another lal was implanted during the exchange.Rxsight's first awareness of the issue was (b)(6) 2021.

• Brand Name: LIGHT ADJUSTABLE LENS (LAL)
• Common Device Name: LIGHT ADJUSTABLE LENS
• Manufacturer (Section D): RXSIGHT, INC.; 100 columbia; aliso viejo CA 92656
• MDR Report Key: 12416165
• Report Number: 3012712027-2021-00048
• Device Sequence Number: 3516009
• Product Code: PZK
• UDI-Device Identifier: 00818806020203
• UDI-Public: 01008188060202031120080717230731
• Combination Product (Y/N): N
• Initial Reporter State: NC
• Initial Reporter Country: US
• PMA/510(K) Number: P160055
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• 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): 09/02/2021

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: 07/31/2023
• Device Model Number: 60005
• Device Catalogue Number: 60005
• Device Lot Number: L02-001776
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 08/30/2021
• Initial Date Received by Manufacturer: 08/05/2021
• Supplement Date Received by Manufacturer: 08/05/2021
• Initial Report FDA Received Date: 09/02/2021
• Supplement Report FDA Received Date: 10/07/2021
• 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