FDA Adverse Event Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3914220 · Received July 3, 2014

Report

Report Number
1531186-2014-02392
Date Received
July 3, 2014
Report Date
June 3, 2014
Manufacturer
UNKNOWN
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER DEALER THE LEFT SIDE WHEEL LOCK IS NOT WORKING FOR THE CONSUMER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
391104 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR UNKNOWN V18PFR

Patients

Seq Age Sex Outcome Treatment
1 Other