FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3011854 · Received March 19, 2013

Report

Report Number
9616091-2013-00472
Event Type
Malfunction
Date Received
March 19, 2013
Report Date
February 20, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATES THE WELD IS BROKEN ON THE LEFT SIDE FRAME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
113525 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX TREX28R

Patients

Seq Age Sex Outcome Treatment
1 Other