FDA Adverse Event Malfunction Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3811742 · Received May 15, 2014

Report

Report Number
1525712-2014-02482
Event Type
Malfunction
Date Received
May 15, 2014
Report Date
December 3, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

CONSUMER ALLEGES THE RIGHT BRAKE IS BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
291186 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other