Events

Recall Or Safety Alert for VESA supports 75/100 for adaptation with rotation, manufactured by ITD GmbH, Germany, used in the articulated arms, references KD.8956.991, KD.8998.991 and KD.8997.991, of the endoscopy carts distributed by Stryker Iberia SL

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 ITD GmbH.

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
    2016-04-04
  • Event Country
    Spain
  • Event Source
    AEMPSVFOI
  • 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
    Replacement of components in certain supports for monitors and articulated arms with VESA 75/100 rotating adapter, manufactured by ITD GmbH, Germany, included in the endoscopy carts distributed by Stryker Corporation, as they do not comply with the specifications.

Device

VESA supports 75/100 for adaptation with rotation, manufactured by ITD GmbH, Germany, used in the...

Manufacturer

ITD GmbH
  • Manufacturer Parent Company (2017)
    Itd Gmbh
  • Source
    AEMPSVFOI