Events

Recall Or Safety Alert for IMMULITE / IMMULITE 1000 IGF-I kit: Lot 055 of the pretreatment solution (LGFA) included in the kit lot 411 of IGF-I I

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 Siemens Healthcare Diagnostics Products Limited.

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
    2016-04-26
  • 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
    Increase in incubation time when using batch 055 of the pretreatment solution (LGFA) included in the lot of kit 411 of IGF-I (Insulin-I growth factor) in the IMMULITE / IMMULITE 1000 Systems, manufactured by Siemens Healthcare Diagnostics Products Limited, United Kingdom.

Device

IMMULITE / IMMULITE 1000 IGF-I kit: Lot 055 of the pretreatment solution (LGFA) included in the k...

Manufacturer

Siemens Healthcare Diagnostics Products Limited
  • Manufacturer Parent Company (2017)
    Siemens AG
  • Source
    AEMPSVFOI