Events

Field Safety Notices about SeQuent Please

According to Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), this field safety notices involved a device in Slovenia that was produced by B. Braun Melsungen AG.

What is this?

Field safety notices are communications sent out by medical device manufacturers or their representatives in relation to actions that they may be taking in relation to their product that is on the market. These are mainly for health workers, but also for users. They can include recalls and alerts.

Learn more about the data here
  • Type of Event
    Field Safety Notice
  • Date
    2016-11-23
  • Event Country
    Slovenia
  • Event Source
    AMPMDRS
  • Notes / Alerts
    Data from Slovenia is current through February 2019. All of the data comes from the Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), 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 Slovenia.
  • Extra notes in the data
  • Reason
    Verification of the batch history record of a complained product revealed that one product of the referenced batch contains a different seouent please catheter than mentioned in the outer prod- uct label. the primary packaging inside the cardboard box may be labelled as and contains a seouent please 2.5 x 15 mm ref 5022206. labelling information in primary packaging may not comply to the information given in the secondary packaging labelling. vascular systems has not received information regarding patient injury in conjunction with this product non—compliance.

Device

SeQuent Please

Manufacturer

B. Braun Melsungen AG