FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3882013 · Received June 18, 2014

Report

Report Number
9616091-2014-01042
Event Type
Malfunction
Date Received
June 18, 2014
Report Date
May 19, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AR, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER ALLEGED THAT THE RIGHT WHEEL IS BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
358987 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9SL

Patients

Seq Age Sex Outcome Treatment
1 52 Other