FDA Adverse Event Malfunction Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3013686 · Received March 20, 2013

Report

Report Number
1525712-2013-02108
Event Type
Malfunction
Date Received
March 20, 2013
Date of Event
February 20, 2013
Report Date
February 20, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

THE DEALER REPORTED THAT THE CONSUMER STATED THE BRAKES ARE NOT FUNCTIONING ON THEIR ROLLATOR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
115290 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other