FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 2914703 · Received January 14, 2013

Report

Report Number
9616091-2013-00077
Event Type
Malfunction
Date Received
January 14, 2013
Date of Event
December 17, 2012
Report Date
January 14, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

A REPORT WAS RECEIVED FROM A DEALER WHO STATES THE TAB WELD MOUNT FOR THE SWINGAWAY ARM BROKE OFF. NO INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
20105 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9XT

Patients

Seq Age Sex Outcome Treatment
1 Other