Notificaciones De Seguridad De Campo acerca de 200ml els syringe for contrast media dosing

Croatian data is current through September 2015. All of the data comes from the Agency for Medical Products and Medical Devices of Croatia, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Croatia.

The Agency for Medicinal Products and Medical Devices (HALMED) has received from the medical device manufacturer MEDTRON AG, Germany, an information about the recall of certain medical device batches 200ml ELS syringe for contrast media dosing.
The manufacturer has provided instructions for users not to use the affected batches.
Here you may view the safety information for users with the list of affected batches.