FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 4132987 · Received October 1, 2014

Report

Report Number
1531186-2014-04615
Date Received
October 1, 2014
Report Date
September 11, 2014
Manufacturer
KENSTONE METAL
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE DEALER ALLEGED THAT A FRONT WHEEL WAS SPLIT. THE DEALER DID NOT PROVIDE ANY FURTHER INFORMATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
612873 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ KENSTONE METAL 66550

Patients

Seq Age Sex Outcome Treatment
1 Other