FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3823591 · Received May 21, 2014

Report

Report Number
9616091-2014-00903
Event Type
Malfunction
Date Received
May 21, 2014
Report Date
April 9, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE WHEEL LOCKS ARE NOT ENGAGING ON A (B)(4) WHEELCHAIR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
302430 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX SOLARA3G

Patients

Seq Age Sex Outcome Treatment
1 Other