FDA Adverse Event Malfunction Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3123278 · Received May 21, 2013

Report

Report Number
1525712-2013-04037
Event Type
Malfunction
Date Received
May 21, 2013
Date of Event
April 22, 2013
Report Date
April 26, 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

CONSUMER ALLEGES THAT HER BRAKES ARE BROKEN ON HER ROLLATOR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
224627 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other