FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3883749 · Received June 19, 2014

Report

Report Number
9616091-2014-01050
Event Type
Malfunction
Date Received
June 19, 2014
Report Date
May 20, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATES ONE OF THE UPPER SUPPORTS ARE MISSING THE RELEASE HARDWARE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
362081 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T4X24RDA

Patients

Seq Age Sex Outcome Treatment
1 Other