FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 4240639 · Received November 10, 2014

Report

Report Number
1531186-2014-05503
Date Received
November 10, 2014
Report Date
October 21, 2014
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER CALLED TO REPORT THEIR CUSTOMER IS REPORTING THE BRAKES ARE BROKE ON BOTH SIDES AND THEY RECEIVED IT THAT WAY UNDER ORDER NUMBER, (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
723367 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65650

Patients

Seq Age Sex Outcome Treatment
1 Other