FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 4241344 · Received November 10, 2014

Report

Report Number
1531186-2014-05498
Date Received
November 10, 2014
Report Date
October 21, 2014
Manufacturer
KENSTONE METAL
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NE, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER REPORTS THAT ROLLATOR WAS RECEIVED DAMAGED. DEALER IS REPORTING THAT THE BACKREST IS BENT INWARD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
723730 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ KENSTONE METAL 66550

Patients

Seq Age Sex Outcome Treatment
1 Other