FDA Adverse Event Death Summary report: N

LTV1150

MDR report key: 23828984 · Received December 17, 2025

Report

Report Number
MW5180692
Event Type
Death
Date Received
December 17, 2025
Date of Event
November 16, 2025
Report Date
December 11, 2025
Manufacturer
VYAIRE MEDICAL, INC.
Product Code
CBK
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
TX, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Description of Event or Problem · 0

PATIENT PASSED AWAY WHILE ON THE VENTILATOR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2039255 LTV1150 VENTILATOR, CONTINUOUS, FACILITY USE CBK VYAIRE MEDICAL, INC. F64852

Patients

Seq Age Sex Outcome Treatment
1 53 YR Male Death