FDA Adverse Event Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3950464 · Received July 22, 2014

Report

Report Number
1531186-2014-02679
Date Received
July 22, 2014
Date of Event
June 12, 2014
Report Date
June 13, 2014
Manufacturer
JUMAO MEDICAL EQUIPMENT
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATES WHEEL IS RUBBING RIGHT SIDE ARM REST, AND THAT RUBBING IS MORE PREVALENT WHEN END USER IS IN CHAIR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
428286 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR JUMAO MEDICAL EQUIPMENT V18RLR

Patients

Seq Age Sex Outcome Treatment
1 Other