MAUDE Adverse Event Report: LUMENIS LTD AcuPulse Duo; Powered Laser Surgical Instrument

Model Number	GA-1000000
Medical Device Problem Code	Fire (1245)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/19/2026
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the fiber went into flames for a second.The case had to be cancelled.
Event or Problem Description
It was reported that the fiber went into flames for a second.The case had to be cancelled.
Event or Problem Description
It was reported that the fiber went into flames for a second.The case had to be cancelled.
Additional Manufacturer Narrative
The device is not available for analysis; therefore, no physical analysis of the product could be performed.The reported device performance allegation cannot be confirmed.The service history confirmed that the problem is considered more likely due to use-related wear or field conditions rather than a potential manufacturing or design issue at the time of release.A risk review was completed and confirmed that the event of fire was defined in the risk documentation and is documented accordingly.This event type has been accounted for during product risk analysis to support acceptable risk benefit for the product.Based on the information available, the cause that contributed to the reported event cannot be established.
Additional Manufacturer Narrative
The device is not available for analysis; therefore, no physical analysis of the product could be performed.The reported device performance allegation cannot be confirmed.The device history record (dhr) confirmed that the device met all material, assembly and performance specifications.The service history confirmed that the problem is considered more likely due to use-related wear or field conditions rather than a potential manufacturing or design issue at the time of release.A risk review was completed and confirmed that the event of fire was defined in the risk documentation and is documented accordingly.This event type has been accounted for during product risk analysis to support acceptable risk benefit for the product.Based on the information available, the cause that contributed to the reported event cannot be established, since the investigation findings do not lead to a clear conclusion about the cause of the reported adverse event.

• Brand Name: AcuPulse Duo
• Common Device Name: Powered Laser Surgical Instrument
• Manufacturer (Section D): LUMENIS LTD; yokneam industrial park; hakidma st 6; yokneam 20692 04; IS 2069204
• Manufacturer (Section G): Lumenis Ltd.; yokneam industrial park; hakidma st 6; yokneam 20692 04; IS 2069204
• Manufacturer Contact: farshad fahimi ; 4100 hamline avenue north; building c; saint paul, MN 55112 ; IS 55112
• MDR Report Key: 25464006
• Report Number: 2124215-2026-31141
• Device Sequence Number: 13352004
• Product Code: GEX
• UDI-Device Identifier: 07290109140292
• UDI-Public: (01)07290109140292(11)210121
• Combination Product (Y/N): N
• Initial Reporter State: MN
• Initial Reporter Country: US
• PMA/510(K) Number: K180597
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 09/03/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: GA-1000000
• Device Catalogue Number: GA-1000000
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/19/2026
• Supplement Date Received by Manufacturer: 07/03/2026; Not provided
• Initial Report FDA Received Date: 06/10/2026
• Supplement Report FDA Received Date: 07/22/2026; 09/03/2026
• Date Device Manufactured: 01/21/2021
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown