FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3961430 · Received July 28, 2014

Report

Report Number
9616091-2014-01319
Event Type
Malfunction
Date Received
July 28, 2014
Date of Event
November 4, 2013
Report Date
June 20, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

END USER'S WIFE ADVISED THE RIGHT SIDE UPPER LEVER BROKE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
438236 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX TREX28R

Patients

Seq Age Sex Outcome Treatment
1 Other