FDA Adverse Event
Death
Summary report: N
MAX VENTILATOR
MDR report key: 231597
·
Received July 1, 1999
Report
- Report Number
- 2937708-1999-00001
- Event Type
- Death
- Date Received
- July 1, 1999
- Date of Event
- May 21, 1999
- Report Date
- June 24, 1999
- Manufacturer
- HAMILTON MEDICAL, INC.
- Product Code
- CBK
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED THAT A PT DIED WHILE BEING VENTILATED WITH A MAX TRANSPORT VENTILATOR. IT IS UNK WHETHER THE DEVICE CONTRIBUTED TO OR WAS ASSOCIATED WITH THE PT INCIDENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MAX VENTILATOR | TRANSPORT VENTILATOR | CBK | HAMILTON MEDICAL, INC. | MAX | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | PULSE-OXIMETER |