FDA Adverse Event Malfunction Summary report: N

WHEELCHAIR ACCESSORY

MDR report key: 3230164 · Received July 16, 2013

Report

Report Number
9616091-2013-01228
Event Type
Malfunction
Date Received
July 16, 2013
Report Date
June 26, 2013
Manufacturer
INVAMEX
Product Code
KNO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OK, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE PROVIDER STATED THE LEVER AND THE FOOTPLATE HAVE ALL BROKEN ON THESE LEGRESTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
329966 WHEELCHAIR ACCESSORY 890.3910 KNO INVAMEX T94HC

Patients

Seq Age Sex Outcome Treatment
1 Other