FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3203023 · Received July 2, 2013

Report

Report Number
9616091-2013-01130
Event Type
Malfunction
Date Received
July 2, 2013
Report Date
June 10, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE PROVIDER REPORTED THE LEFT FRONT CASTER FORK ON THE SOLARA3G MANUAL WHEELCHAIR IS BENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
303062 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX SOLARA3G

Patients

Seq Age Sex Outcome Treatment
1 Other