Recall Or Safety Alert for "Universal SlingBar 350" sling bars (3156074, 3156084 and 3156094), "Universal SlingBar 450" (3156075, 3156085 and 3156095) and "Universal SlingBar 600" (3156076 and 3156086), manufactured until May 2014

According to Agencia Española de Medicamentos y Productos Sanitarios (Via FOI), this recall or safety alert involved a device in Spain that was produced by Liko AB.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

Learn more about the data here
  • Type of Event
    Recall / Safety Alert
  • Date
  • Event Country
  • Event Source
  • Notes / Alerts
    The data from Spain is current through June 2018. All of the data comes from Agencia Española de Medicamentos y Productos Sanitarios, 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 Spain.
  • Extra notes in the data
  • Action
    Possibility that the central screw of the sling bars "Universal SlingBar 350", "Universal SlingBar 450" and "Universal SlingBar 600", manufactured by Liko AB, Sweden, breaks and the patient falls.