FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 2933969 · Received January 29, 2013

Report

Report Number
9616091-2013-00133
Event Type
Malfunction
Date Received
January 29, 2013
Report Date
January 29, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MS, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATES BROKEN WELD IS ON THE LEFT SIDE OF THE FRAME. NO INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
38903 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T424RDA

Patients

Seq Age Sex Outcome Treatment
1 Other