FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3952720 · Received July 23, 2014

Report

Report Number
1531186-2014-02718
Date Received
July 23, 2014
Date of Event
June 13, 2014
Report Date
June 16, 2014
Manufacturer
KENSTONE METAL
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE LEFT BRAKE CABLE BROKE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
431660 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ KENSTONE METAL 66550

Patients

Seq Age Sex Outcome Treatment
1 Other