FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3953057 · Received July 23, 2014

Report

Report Number
9616091-2014-01283
Event Type
Malfunction
Date Received
July 23, 2014
Report Date
June 16, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER ALLEGED THAT THE RIGHT REAR WHEEL IS WOBBLY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
431064 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T422RDA

Patients

Seq Age Sex Outcome Treatment
1 Other