FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3200383 · Received July 1, 2013

Report

Report Number
1525712-2013-05219
Event Type
Malfunction
Date Received
July 1, 2013
Report Date
June 6, 2013
Manufacturer
UNKNOWN
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE PROVIDER REPORTED THE BRAKE ON THE SOLARA3G MANUAL WHEELCHAIR IS LOOSE AND NOT LOCKING PROPERLY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
300241 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR UNKNOWN SOLOARA3G

Patients

Seq Age Sex Outcome Treatment
1 Other