FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3163525 · Received June 11, 2013

Report

Report Number
1525712-2013-04550
Event Type
Malfunction
Date Received
June 11, 2013
Report Date
May 14, 2013
Manufacturer
UNKNOWN
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

DEALER ALLEGES THE TORSION SPRING BROKE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
263906 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other