FDA Adverse Event Injury Summary report: N

LIGHT ADJUSTABLE LENS (LAL)

MDR report key: 13049052 · Received December 20, 2021

Report

Report Number
3012712027-2021-00086
Event Type
Injury
Date Received
December 20, 2021
Date of Event
October 15, 2021
Report Date
December 15, 2021
Manufacturer
RXSIGHT, INC.
Product Code
PZK
UDI-DI
00818806020258
PMA / PMN Number
P160055
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

SITE REPORTED THAT A LIGHT ADJUSTABLE LENS WAS EXPLANTED FROM THE PATIENT AS THE PATIENT WAS EXPERIENCING DOUBLE VISION. RXSIGHT'S FIRST AWARENESS OF THE EVENT WAS 12/1/2021. THE EXPLANTED LENS WAS RETURNED FOR EVALUATION. VISUAL INSPECTION AND OPTICAL TESTING OF THE RETURNED LENS CONFIRMED THE PRESENCE OF AN AMBIENT ZONE ON THE LENS, WHICH IS INDICATIVE OF EXPOSURE OF THE LENS TO AMBIENT UV LIGHT PRIOR TO LOCK IN.

Additional Manufacturer Narrative · 0

SITE REPORTED THAT A LIGHT ADJUSTABLE LENS WAS EXPLANTED FROM THE PATIENT 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 LENS IS IN THE PROCESS OF BEING RETURNED FOR EVALUATION.

Description of Event or Problem · 0

SITE REPORTED THAT A LIGHT ADJUSTABLE LENS WAS EXPLANTED FROM THE PATIENT AS THE PATIENT WAS EXPERIENCING DOUBLE VISION. RXSIGHT'S FIRST AWARENESS OF THE EVENT WAS 12/1/2021.

Description of Event or Problem · 0

SITE REPORTED THAT A LIGHT ADJUSTABLE LENS WAS EXPLANTED FROM THE PATIENT AS THE PATIENT WAS EXPERIENCING DOUBLE VISION. RXSIGHT'S FIRST AWARENESS OF THE EVENT WAS (B)(6) 2021.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1947497 LIGHT ADJUSTABLE LENS (LAL) LIGHT ADJUSTABLE LENS PZK RXSIGHT, INC. 60005 L02-001664 00818806020258

Patients

Seq Age Sex Outcome Treatment
1 Female Required Intervention