FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3882096 · Received June 18, 2014

Report

Report Number
1531186-2014-02163
Date Received
June 18, 2014
Date of Event
May 16, 2014
Report Date
May 19, 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

DEALER ALLEGED THE LEFT CABLE BROKE WHERE IT ATTACHES TO THE HANDLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
358567 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ KENSTONE METAL 65350GR

Patients

Seq Age Sex Outcome Treatment
1 Other