FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3973226 · Received August 1, 2014

Report

Report Number
1531186-2014-02762
Date Received
August 1, 2014
Date of Event
June 4, 2014
Report Date
June 18, 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

PER DEALER, THE BRAKES ARE NOT HOLDING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
451181 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ KENSTONE METAL 66550

Patients

Seq Age Sex Outcome Treatment
1 Other