FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3980768 · Received August 5, 2014

Report

Report Number
1531186-2014-02988
Date Received
August 5, 2014
Report Date
July 3, 2014
Manufacturer
CONSMA
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

END USER SPOUSE STATES THAT THE FRAME BENT AT THE WELD, NEAR THE WHEELS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
457962 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ CONSMA 65650R

Patients

Seq Age Sex Outcome Treatment
1 Other