FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 2990189 · Received March 5, 2013

Report

Report Number
9616091-2013-00350
Event Type
Malfunction
Date Received
March 5, 2013
Report Date
February 6, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(4). THE DEALER REPORTED THAT THE PATIENT WAS RIDING A TRSX50FB MECHANICAL WHEELCHAIR HAVING WORN BEARINGS. THERE WAS NO PATIENT INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
93478 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX TRSX50FB

Patients

Seq Age Sex Outcome Treatment
1 Other