FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 4240801 · Received November 10, 2014

Report

Report Number
9616091-2014-02417
Event Type
Malfunction
Date Received
November 10, 2014
Report Date
October 22, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATES THE BOLT THAT HOLDS THE WHEEL LOCK ON, BROKE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
722621 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX TREX28RP

Patients

Seq Age Sex Outcome Treatment
1 Other