FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3211922 · Received July 8, 2013

Report

Report Number
9616091-2013-01159
Event Type
Malfunction
Date Received
July 8, 2013
Report Date
June 13, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
RI, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATES FRONT RIGGING PART HAS FALLEN OFF AND WILL NOT GO BACK ON; IT PREVENTS THE RAISING AND LOWERING OF THE LEGREST.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
309656 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T4X24RDA

Patients

Seq Age Sex Outcome Treatment
1 Other