FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3180994 · Received June 20, 2013

Report

Report Number
1531186-2013-02717
Date Received
June 20, 2013
Report Date
May 24, 2013
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 ALLEGES THE CABLES SNAPPED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
280745 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ KENSTONE METAL 65650

Patients

Seq Age Sex Outcome Treatment
1 Other