FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 2840992 · Received November 20, 2012

Report

Report Number
1531186-2012-01416
Date Received
November 20, 2012
Report Date
November 17, 2012
Manufacturer
CONSMA
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VT, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATED THAT THE BRAKE CABLE IS NO LONGER ATTACHED TO THE HANDLE. IN SPEAKING WITH THE REPORTER IT WAS LEARNED THAT THERE WAS NO HARM AND THE REPAIR HAS BEEN COMPLETED WITHOUT FURTHER INCIDENT.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 52 YR Other