FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3211921 · Received July 8, 2013

Report

Report Number
9616091-2013-01158
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
IL, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATES ON THE RIGHT SIDE OF THE FRAME WHERE THE PINS ARE LOCATED IS BENT AND FRONT RIGGING CAN NOT BE ATTACHED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
311199 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9XT

Patients

Seq Age Sex Outcome Treatment
1 Other