FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3886911 · Received June 20, 2014

Report

Report Number
1531186-2014-02206
Date Received
June 20, 2014
Report Date
May 21, 2014
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

PER END USER THE CASTER IS BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
363461 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65350GR

Patients

Seq Age Sex Outcome Treatment
1 Other