FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3191812 · Received June 26, 2013

Report

Report Number
9616091-2013-01085
Event Type
Malfunction
Date Received
June 26, 2013
Report Date
May 31, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATES FRAME IS BENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
290984 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9XDT

Patients

Seq Age Sex Outcome Treatment
1 Other