FDA Adverse Event Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3233098 · Received July 18, 2013

Report

Report Number
1531186-2013-03208
Date Received
July 18, 2013
Report Date
June 26, 2013
Manufacturer
JUMAO MEDICAL EQUIPMENT
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE PROVIDER STATED THE WHEEL BROKE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
333418 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR JUMAO MEDICAL EQUIPMENT V20RFR

Patients

Seq Age Sex Outcome Treatment
1 Other