FDA Adverse Event Summary report: N

DAILY ACTIVITY ASSIST DEVICES

MDR report key: 3844578 · Received June 3, 2014

Report

Report Number
1531186-2014-02055
Date Received
June 3, 2014
Report Date
February 20, 2014
Manufacturer
RALON MEDICAL EQUIPMENT CO. LTD.
Product Code
ILS
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATED THAT THE ARM ON A 6599 BARIATRIC COMMODE WAS BROKEN, OUT OF THE BOX.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
323975 DAILY ACTIVITY ASSIST DEVICES 890.5050 ILS RALON MEDICAL EQUIPMENT CO. LTD. 6599

Patients

Seq Age Sex Outcome Treatment
1 Other