FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3133246 · Received May 29, 2013

Report

Report Number
1531186-2013-02341
Date Received
May 29, 2013
Report Date
December 5, 2012
Manufacturer
KENSTONE METAL
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
DE, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). COMPLAINT WAS NOT GIVEN TO REGULATORY AFFAIRS FOR PROCESSING UNTIL (B)(4) 2013.

Description of Event or Problem · 1

THE DEALER REPORTS THE BRAKES ARE BAD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
236946 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ KENSTONE METAL 66550

Patients

Seq Age Sex Outcome Treatment
1 Other