FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3253380 · Received July 29, 2013

Report

Report Number
9616091-2013-01360
Event Type
Malfunction
Date Received
July 29, 2013
Report Date
July 12, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE DEALER STATES THE BACK CANE IS BENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
353203 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX TREX28R

Patients

Seq Age Sex Outcome Treatment
1 Other