MAUDE Adverse Event Report: Verathon Medical ULC GlideScope Core 15-inch FHD Monitor; LARYNGOSCOPE, RIGID

Model Number	0570-0437
Medical Device Problem Codes	Power Problem (3010); Intermittent Loss of Power (4016)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/21/2026
Type of Reportable Event	Malfunction
Event or Problem Description
A customer reported that while using a glidescope core 15-inch fhd monitor, the device unexpectedly shut down in the middle of the procedure.No delay in procedure, use of a backup device, or harm to the patient was reported.The end user noted that the battery was fully charged when the shut down occurred.Following the reported event, the facility's biomedical engineering representative was unable to reproduce the reported issue.
Additional Manufacturer Narrative
The reported glidescope core 15-inch fhd monitor was returned to verathon for evaluation along with the glidescope core smart cable used during the reported event.A verathon technical service representative evaluated the returned devices but was unable to confirm the reported premature shut down issue.When connecting the monitor to verathon's test equipment, no power issues were observed.The monitor passed visual inspection and verathon's device functionality testing, confirmed to be operating within specification.Upon completion of verathon's device evaluation, both the monitor and smart cable were returned to the customer.No further investigation is required at this time.Verathon will continue to monitor trends.

• Brand Name: GlideScope Core 15-inch FHD Monitor
• Common Device Name: LARYNGOSCOPE, RIGID
• Manufacturer (Section D): Verathon Medical ULC; 2227 douglas road; burnaby, british columbia V5C5A 9; CA V5C5A9
• Manufacturer (Section G): Verathon Medical ULC; 2227 douglas road; burnaby, british columbia V5C5A 9; CA V5C5A9
• Manufacturer Contact: corey kasbohm ; 20001 n creek pkwy; bothell, WA 98011--821 ; +1(425)629-5760
• MDR Report Key: 50776917
• Report Number: 9615393-2026-00135
• Device Sequence Number: 10708066
• Product Code: CCW
• UDI-Device Identifier: 00879123008596
• UDI-Public: (01)00879123008596(11)240108
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• PMA/510(K) Number: Exempt
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility
• Initial Reporter Occupation: Biomedical Engineer
• Type of Report: Initial
• Report Date (Section B): 09/15/2026

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: 0570-0437
• Device Catalogue Number: 0270-1033-FHD
• Device Lot Number: N/A
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 08/27/2026
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/21/2026
• Initial Report FDA Received Date: 09/15/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 01/08/2024
• 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