FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3072047 · Received April 22, 2013

Report

Report Number
9616091-2013-00685
Event Type
Malfunction
Date Received
April 22, 2013
Report Date
March 28, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATED CROSSBRACES ARE BROKEN DUE TO ABUSE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
172530 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9XT

Patients

Seq Age Sex Outcome Treatment
1 Other