FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3901989 · Received June 30, 2014

Report

Report Number
1531186-2014-02292
Date Received
June 30, 2014
Date of Event
May 23, 2014
Report Date
May 28, 2014
Manufacturer
KENSTONE METAL
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE DEALER ALLEGES THAT THE BRAKE CABLE BROKE INSIDE OF THE HANDLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
380974 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ KENSTONE METAL 65650

Patients

Seq Age Sex Outcome Treatment
1 Other