FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 2940436 · Received February 3, 2013

Report

Report Number
1531186-2013-00371
Date Received
February 3, 2013
Report Date
January 31, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATES BACKREST IS LOOSE FROM FRAME. SERVICE TECHNICIAN TRIED TO TIGHTEN BUT WAS NOT SUCCESSFUL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
45856 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65851

Patients

Seq Age Sex Outcome Treatment
1 Other