FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3243472 · Received July 23, 2013

Report

Report Number
1525712-2013-06060
Event Type
Malfunction
Date Received
July 23, 2013
Report Date
July 3, 2013
Manufacturer
UNKNOWN
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

ALLEGEDLY TILT CABLE WILL NOT RELEASE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
343088 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR UNKNOWN SOLARA

Patients

Seq Age Sex Outcome Treatment
1 Other