FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 4120168 · Received September 25, 2014

Report

Report Number
1531186-2014-04468
Date Received
September 25, 2014
Report Date
September 5, 2014
Manufacturer
EUROCHARM INNOVATION CO., LTD
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER DEALER, BRAKE CABLE SNAPPED WHERE IT MEETS THE HANDLE. NO PARTS AVAILABLE

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
598885 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ EUROCHARM INNOVATION CO., LTD 65420

Patients

Seq Age Sex Outcome Treatment
1 Other