FDA Adverse Event Death Summary report: N

PRECISION MEDICAL POWER VAC

MDR report key: 673661 · Received February 8, 2006

Report

Report Number
2523148-2006-00002
Event Type
Death
Date Received
February 8, 2006
Date of Event
January 26, 2006
Report Date
February 7, 2006
Manufacturer
PRECISION MEDICAL INC
Product Code
BTA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
INVALID DATA

Narratives

Description of Event or Problem · 1

PATIENT'S DAUGHTER IS ALLEGING THAT THE SUCTION DEVICE WAS NOT WORKING CORRECTLY, AND THIS CONTRIBUTED TO THE PATIENT'S DEATH.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PRECISION MEDICAL POWER VAC PORTABLE SUCTION DEVICE BTA PRECISION MEDICAL INC PM63 *

Patients

Seq Age Sex Outcome Treatment
1 * Death