FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3840926 · Received May 30, 2014

Report

Report Number
9616091-2014-00957
Event Type
Malfunction
Date Received
May 30, 2014
Report Date
April 16, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

CUSTOMER ALLEGES THE WHEEL IS HITTING THE ARM REST UNEVENLY DUE TO THE WHEELS BEING WARPED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
318364 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T4

Patients

Seq Age Sex Outcome Treatment
1 Other