FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3903247 · Received June 30, 2014

Report

Report Number
9616091-2014-01103
Event Type
Malfunction
Date Received
June 30, 2014
Report Date
May 28, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER ALLEGED THAT THE CASTER WHEELS ARE FLEXED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
380111 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX SL2028F

Patients

Seq Age Sex Outcome Treatment
1 Other