Date Issued: January 4, 2021
Baxter Healthcare Recalls Baxter SIGMA Spectrum Infusion Pumps with Master Drug Library (Versions 6 and 8) and Spectrum IQ Infusion Systems with Dose IQ Safety Software Due to Unplanned Shutdown Issues
KCER Release Date: September 4, 2020
BD Provides Update on Previously Disclosed Recall of BD Alaris System Hardware
Check out our new interactive page to search for Kidney Transplant programs in the Midwest Kidney Network region.
July 31, 2020
May 30, 2020
Use the Correct Cycle and Compatible N95 Respirators When Decontaminating Respirators with STERRAD Sterilization Systems - Letter to Health Care Providers
April 22, 2020
Important Information on the Use of Serological (Antibody) Tests for COVID-19 - Letter to Health Care Providers
ISSUE: The FDA announced it is requesting manufacturers to withdraw all prescription and over-the-counter (OTC) ranitidine drugs from the market immediately.
April 1, 2020
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
March 30, 2020
Distributed via the CDC Health Alert Network