FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3790312 · Received May 5, 2014

Report

Report Number
9616091-2014-00815
Event Type
Malfunction
Date Received
May 5, 2014
Date of Event
April 3, 2014
Report Date
April 3, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AL, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATED THAT THE LEFT REAR FRAME ON A T4 WHEELCHAIR HAS BROKEN AT A WELD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
266459 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T4

Patients

Seq Age Sex Outcome Treatment
1 53 Other