FDA MedWatch: Infusion Pump Battery Recall: ICU Medical Removes Some CSB Batteries Intended For Use With Plum 360, A+, and A+3 Infusion Systems Due to Reports of Allegedly Counterfeit, Untested Batteries In Use
FDA MedWatch: Hemodialysis Correction: Baxter Issues Correction for AK 98 Hemodialysis Machines Due to Risk of Patient Exposure to Higher Than Allowable Levels of Toxic Compound NDL-PCBA and/or NDL-PCBs
Baxter North Cove Facility and Associated Product Disruptions
FDA Medical Device Recall Infusion Pump Administration Set Recall: Fresenius Kabi USA Removes Certain Ivenix Large Volume Pump Primary Administration Sets
PRESS RELEASE - Superior Health Quality Alliance Plans for CMS 13th Statement of Work and Unveils Enhanced Website
Introducing Dialysis Office Hours – Monthly NHSN Tips and Trainings
Infusion Pump Battery Correction: ICU Medical Updates Instructions for Use Regarding Batteries in Plum 360, A+ and A+3 Infusion System due to Diminished Battery Life that May Impact Infusion Delivery
Updated CMS 2728 Oct release and EQRS
Disruption in Availability of BD BACTEC Blood Culture Media Bottles – Letter to Health Care Providers

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