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 |