FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3100695 · Received May 8, 2013

Report

Report Number
1531186-2013-01953
Date Received
May 8, 2013
Report Date
April 11, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER PROVIDER THE TABS ON THE INSIDE OF THE BACKREST HAVE BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
200400 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65650

Patients

Seq Age Sex Outcome Treatment
1 Other