FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3112806 · Received May 14, 2013

Report

Report Number
1525712-2013-03796
Event Type
Malfunction
Date Received
May 14, 2013
Report Date
April 18, 2013
Manufacturer
UNKNOWN
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER PROVIDER ELEVATING LEGS WILL NOT GO BACK DOWN AFTER BEING ELEVATED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
213233 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR UNKNOWN T94HE

Patients

Seq Age Sex Outcome Treatment
1 Other