FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 4191679 · Received October 22, 2014

Report

Report Number
1531186-2014-04993
Date Received
October 22, 2014
Date of Event
September 29, 2014
Report Date
September 30, 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 STATES THAT THE CABLES HAVE BROKEN OFF. DEALER ALLEGES THAT IT JUST BROKE OFF.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
674241 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ KENSTONE METAL 66550

Patients

Seq Age Sex Outcome Treatment
1 Other