FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 4211439 · Received October 29, 2014

Report

Report Number
1525712-2014-07394
Event Type
Malfunction
Date Received
October 29, 2014
Report Date
October 9, 2014
Manufacturer
UNKNOWN
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE PROVIDER STATES THE WELDS ON THE FRONT RIGGING HAVE BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
694031 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR UNKNOWN TOPENDPARTS

Patients

Seq Age Sex Outcome Treatment
1 Other