FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3951164 · Received July 22, 2014

Report

Report Number
9616091-2014-01267
Event Type
Malfunction
Date Received
July 22, 2014
Report Date
June 17, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER PROVIDER, BROKEN CROSSBRACE AT THE WELD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
428000 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9SL

Patients

Seq Age Sex Outcome Treatment
1 Other