MAUDE Adverse Event Report: Stryker Endoscopy-San Jose PKG CROSSFIRE 2 CONSOLE; electrosurgical, cutting & coagulation & accessories

Catalog Number	0475100000
Medical Device Problem Code	Fire (1245)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/14/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Additional information will be provided once the investigation has been completed.The device manufacturer date is not known at this time.However, should it become available it will be provided in future reports.
Event or Problem Description
It was reported that the crossfire 2 console caught on fire mid-procedure after rf wand was activated.
Event or Problem Description
It was reported that the crossfire 2 console caught on fire mid procedure after rf wand was activated.
Additional Manufacturer Narrative
Product was not received in-house at stryker endoscopy.This complaint investigation was closed based on the device not received, therefore the reported failure mode was not confirmed.In the event that the device is received, the complaint will be reopened and the investigation will be updated with new results.Alleged failure: console caught on fire mid procedure: probable root cause: console fuses fail to break circuit due to excessive mains current leading to fire, isolation power supply failure, use error: console is sterilized or disinfected, use error: console cleaned with incompatible products.The reported failure mode will be monitored for future reoccurrence.

• Brand Name: PKG CROSSFIRE 2 CONSOLE
• Common Device Name: electrosurgical, cutting & coagulation & accessories
• Manufacturer (Section D): Stryker Endoscopy-San Jose; 5900 optical court; san jose CA 95138
• Manufacturer (Section G): Stryker Endoscopy-San Jose; 5900 optical court; san jose CA 95138
• Manufacturer Contact: arsalan rizvi ; 5900 optical court; san jose, CA 95138 ; +1(408)754-2000
• MDR Report Key: 25476779
• Report Number: 0002936485-2026-00373
• Device Sequence Number: 9165574
• Product Code: GEI
• UDI-Device Identifier: 07613327058109
• UDI-Public: (01)07613327058109
• Combination Product (Y/N): N
• Initial Reporter State: PA
• Initial Reporter Country: US
• PMA/510(K) Number: K071859
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Type of Report: Initial,Followup
• Report Date (Section B): 09/18/2026

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 Catalogue Number: 0475100000
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 05/14/2026
• Supplement Date Received by Manufacturer: 08/28/2026
• Initial Report FDA Received Date: 06/11/2026
• Supplement Report FDA Received Date: 09/18/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• 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