FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3200351 · Received July 1, 2013

Report

Report Number
9616091-2013-01111
Event Type
Malfunction
Date Received
July 1, 2013
Report Date
June 6, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

PROVIDER STATES FOOTPLATE BROKE THAT HOLDS IT UP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
299773 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX TRSX5

Patients

Seq Age Sex Outcome Treatment
1 Other