MAUDE Adverse Event Report: VERATHON MEDICAL ULC GLIDESCOPE SPECTRUM QC ECO HYPERANGLE S3, NON-STERILE; LARYNGOSCOPE, RIGID

Model Number	0574-0267
Medical Device Problem Codes	No Display/Image (1183); Display or Visual Feedback Problem (1184)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/11/2026
Type of Reportable Event	Malfunction
Event or Problem Description
A customer reported while using a glidescope spectrum qc eco hyperangle s3, non-sterile blade during a patient procedure, the light source went dark when they placed it in the patient's mouth.They switched to a glidescope spectrum qc eco, hyperangle s4 with the same monitor and cable which worked as intended.Switching to the alternative blade delayed the procedure by approximately 30 seconds to one (1) minute.No harm to the patient was reported.
Additional Manufacturer Narrative
The glidescope spectrum qc eco hyperangle s3, non-sterile blade was returned to verathon for evaluation along with two other blades from different lots.A verathon technical service representative evaluated the device and was able to confirm that one of the three blades had no led powering on.All three blades displayed image as expected.Visual inspection did not identify any damage.The blade failed verathon's device functionality testing.Upon completion of verathon's device evaluation, the blade was scrapped due to being a single-use device and the customer already being provided replacement blades by their verathon territory manager.Corrective action is not required at this time.Verathon will continue to monitor for trends.

• Brand Name: GLIDESCOPE SPECTRUM QC ECO HYPERANGLE S3, NON-STERILE
• Common Device Name: LARYNGOSCOPE, RIGID
• Manufacturer (Section D): VERATHON MEDICAL ULC; 2227 douglas road; burnaby, british columbia V5C 5 A9; CA V5C 5A9
• Manufacturer (Section G): VERATHON MEDICAL ULC; 2227 douglas road; burnaby, british columbia V5C 5 A9; CA V5C 5A9
• Manufacturer Contact: corey kasbohm ; 20001 n creek pkwy; bothell, WA 98011-8218 ; 4256295760
• MDR Report Key: 25738085
• Report Number: 9615393-2026-00100
• Device Sequence Number: 10412654
• Product Code: CCW
• UDI-Device Identifier: 00879123009197
• UDI-Public: (01)00879123009197(10)QP1024216(11)260415(17)290415
• 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,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 07/07/2026

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: 0574-0267
• Device Catalogue Number: 0270-1145
• Device Lot Number: QP1024216
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 06/22/2026
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/11/2026
• Initial Report FDA Received Date: 07/07/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 04/15/2026
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown