Safety Alert for MG MAGNESIUM FLEX® REAGENT CARTRIDGE

According to National Institute of Drugs and Food Surveillance (INVIMA), this safety alert involved a device in Colombia that was produced by Siemens HealthCare Diagnostics || Importer: Siemens Healthcare Colombia.

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
    Safety alert
  • Event ID
    RRD-031015
  • Event Number
    INVIMA 2006RD-0000114
  • Date
    2015-10-22
  • Event Country
  • Event Source
    INVIMA
  • Event Source URL
  • Notes / Alerts
    Colombian data is current through June 2019. All of the data comes from the National Institute of Drugs and Food Surveillance (INVIMA), 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 Colombia.
  • Extra notes in the data
  • Reason
    Claims from clients in relation to results that are loosely low in a small number of reagents. when this problem occurs, the low recovery of quality control varies from -0.3 mg / dl to -1.6 mg / dl. the mean value for the low recovery value is -1.0 mg / dl. this incident appears to occur with a frequency of 1 in 10,000 tests.

Device

Manufacturer