FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3203612 · Received July 3, 2013

Report

Report Number
9616091-2013-01132
Event Type
Malfunction
Date Received
July 3, 2013
Report Date
June 10, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE PROVIDER REPORTED THE CASTER IS BROKEN AT THE RIGHT SPOKE OF THE 9SL_PTO_47874 MANUAL WHEELCHAIR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
304272 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9SL_PTO_47874

Patients

Seq Age Sex Outcome Treatment
1 Other