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