FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3932605 · Received July 14, 2014

Report

Report Number
9616091-2014-01198
Event Type
Malfunction
Date Received
July 14, 2014
Report Date
June 6, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
ID, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATED THAT NOT ALL 4 WHEELS ON A TREX20RP WHEELCHAIR TOUCH THE GROUND AT THE SAME TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
409539 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX TREX20RP

Patients

Seq Age Sex Outcome Treatment
1 Other