FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3954438 · Received July 24, 2014

Report

Report Number
1525712-2014-03955
Event Type
Malfunction
Date Received
July 24, 2014
Report Date
June 16, 2014
Manufacturer
UNKNOWN
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 STATES THE BEARINGS ARE PUSHED IN CAUSING IT TO RUB AGAINST THE FRAME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
434685 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other