FDA Adverse Event Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3180989 · Received June 20, 2013

Report

Report Number
1531186-2013-02712
Date Received
June 20, 2013
Report Date
May 24, 2013
Manufacturer
JUMAO MEDICAL EQUIPMENT
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OR, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATES BROKEN WELD ON CASTER HEADTUBE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
280511 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR JUMAO MEDICAL EQUIPMENT TREX26R

Patients

Seq Age Sex Outcome Treatment
1 Other