FDA Adverse Event Injury Summary report: N

ENLIGHTEN III

MDR report key: 22081619 · Received May 23, 2025

Report

Report Number
2954354-2025-00003
Event Type
Injury
Date Received
May 23, 2025
Report Date
May 23, 2025
Manufacturer
CUTERA, INC.
Product Code
GEX
UDI-DI
00816722021649
PMA / PMN Number
K182997
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
003

Narratives

Description of Event or Problem · 0

CUTERA, INC., RECEIVED A REPORT FROM A CLINIC INDICATING THAT A LASER TECHNICIAN SUSTAINED AN OCULAR INJURY ("PUPIL BURN") DURING A TATTOO REMOVAL PROCEDURE INVOLVING THE ENLIGHTEN III LASER SYSTEM AND AN UNSPECIFIED "PATCH." ACCORDING TO THE CLINIC, THE TECHNICIAN WAS STRUCK IN THE EYE BY A LASER BEAM "THAT REFLECTED OFF THE PATCH" AND WAS NOT WEARING PROTECTIVE EYEWEAR AT THE TIME OF THE INCIDENT. FOLLOWING THE INJURY, THE TECHNICIAN WAS REFERRED TO A SPECIALIST AND DIAGNOSED WITH A BURN TO THE PUPIL. BASED ON THE INFORMATION PROVIDED, THE INCIDENT APPEARS TO INVOLVE OPERATOR ERROR, SPECIFICALLY THE FAILURE TO USE APPROPRIATE EYE PROTECTION AS REQUIRED BY THE ENLIGHTEN III INSTRUCTIONS FOR USE (IFU). THE CLINIC REPORTED THAT THE LASER BEAM REFLECTED OFF THE "PATCH" USED DURING THE PROCEDURE; HOWEVER, NO ADDITIONAL INFORMATION REGARDING THE BRAND OR SPECIFICATIONS OF THE PATCH WAS PROVIDED. THE ENLIGHTEN III IFU INCLUDES EXPLICIT WARNINGS REGARDING THE CRITICAL IMPORTANCE OF PROTECTIVE EYEWEAR FOR ALL INDIVIDUALS PRESENT DURING LASER OPERATION. HOWEVER, THE IFU DOES NOT ADDRESS THE USE OF THIRD-PARTY PATCHES IN CONJUNCTION WITH THE ENLIGHTEN III LASER SYSTEM. THERE HAS BEEN NO INDICATION OF ENLIGHTEN III LASER SYSTEM MALFUNCTION OR FAILURE. TO DATE, CUTERA HAS NOT RECEIVED ANY OTHER REPORTS OF EYE INJURIES OCCURRING WHEN THE RECOMMENDED PROTECTIVE EYEWEAR WAS USED CORRECTLY. THE EVENT WAS MOST LIKELY THE RESULT OF USER NON-COMPLIANCE WITH STANDARD LASER SAFETY PROTOCOLS. THE ABSENCE OF PROTECTIVE EYEWEAR AND THE USE OF AN UNVERIFIED THIRD-PARTY PATCH MAY HAVE CONTRIBUTED TO THE REFLECTION AND SUBSEQUENT INJURY. CUTERA HAS TAKEN THE FOLLOWING ACTIONS IN RESPONSE TO THIS EVENT: - ISSUED A FORMAL RESPONSE TO THE CLINIC REITERATING THE IMPORTANCE OF USING PROCEDURE-APPROPRIATE PROTECTIVE EYEWEAR. - PROVIDED A SUMMARY OF EYE HAZARDS ASSOCIATED WITH CLASS IV MEDICAL LASERS AND PRECAUTIONS FOR INJURY PREVENTION. - RECOMMENDED REVIEW OF ANSI Z136.3 - AMERICAN NATIONAL STANDARD FOR SAFE USE OF LASERS IN HEALTH CARE FACILITIES. - SUPPLIED LINKS TO CERTIFIED LASER SAFETY TRAINING COURSES TAILORED TO MEDICAL PROFESSIONALS. - SHARED THE ENLIGHTEN III OPERATOR MANUAL AND TREATMENT GUIDELINES, EMPHASIZING SECTIONS RELATED TO PROTECTIVE EYEWEAR AND SAFETY PROTOCOLS. - OFFERED A CLINICAL EDUCATION SESSION WITH CUTERA'S CLINICAL APPLICATIONS SPECIALISTS TO REVIEW SELECTION OF PROTECTIVE EYEWEAR. - ADVISED THE CLINIC TO REPORT THE INCIDENT TO THE MANUFACTURER OF THE PATCH USED DURING THE PROCEDURE. THE CLINIC DID NOT DISCLOSE THE DATE OF THE PROCEDURE, NOR HAS IT PROVIDED ANY SUPPLEMENTAL DETAILS BEYOND THE INITIAL INCIDENT REPORT SUBMITTED TO CUTERA. THIS MEDICAL DEVICE REPORT IS BEING FILED IN GOOD FAITH BASED SOLELY ON THE LIMITED INFORMATION AVAILABLE FROM THE CLINIC AT THE TIME OF REPORTING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
326418 ENLIGHTEN III POWERED LASER SURGICAL INSTRUMENT GEX CUTERA, INC. 00816722021649

Patients

Seq Age Sex Outcome Treatment
1 NA Female Other| R