FDA Adverse Event Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3230122 · Received July 16, 2013

Report

Report Number
1531186-2013-03182
Date Received
July 16, 2013
Report Date
June 25, 2013
Manufacturer
JUMAO MEDICAL EQUIPMENT
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE DEALER REPORTS THE FRAME OR AXLE IS BENT, BOTH ITEMS ARE NOT SALEABLE PARTS. THE CHAIR HAS TO BE REPLACED. NON WARRANTY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
328729 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR JUMAO MEDICAL EQUIPMENT V16RFR

Patients

Seq Age Sex Outcome Treatment
1 Other