FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3981523 · Received August 5, 2014

Report

Report Number
1531186-2014-03006
Date Received
August 5, 2014
Date of Event
June 26, 2014
Report Date
July 1, 2014
Manufacturer
KENSTONE METAL
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AL, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER ADVISED RIGHT BRAKE IS NOT WORKING PROPERLY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
457113 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ KENSTONE METAL 66550

Patients

Seq Age Sex Outcome Treatment
1 Other