FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 4090009 · Received September 15, 2014

Report

Report Number
1531186-2014-04112
Date Received
September 15, 2014
Report Date
August 19, 2014
Manufacturer
KENSTONE METAL
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MT, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER ALLEGED RIGHT SIDE BRAKE CABLE IS FRAYED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
570394 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ KENSTONE METAL 66550

Patients

Seq Age Sex Outcome Treatment
1 Other