FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 4140728 · Received October 3, 2014

Report

Report Number
9616091-2014-02082
Event Type
Malfunction
Date Received
October 3, 2014
Report Date
September 15, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER ALLEGED SEAT UPHOLSTERY IS BUNCHING UP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
619847 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9XT

Patients

Seq Age Sex Outcome Treatment
1 Other