FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3950383 · Received July 22, 2014

Report

Report Number
9616091-2014-01276
Event Type
Malfunction
Date Received
July 22, 2014
Report Date
June 16, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY THE CUSTOMER THAT THE WHEEL LOCKS ARE DIFFICULT TO ENGAGE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
427591 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX TREX20PP

Patients

Seq Age Sex Outcome Treatment
1 Other