FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 4103305 · Received September 19, 2014

Report

Report Number
1525712-2014-06074
Event Type
Malfunction
Date Received
September 19, 2014
Report Date
August 29, 2014
Manufacturer
UNKNOWN
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OK, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE PROVIDER STATES THE WHEEL IS WOBBLY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
583604 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other