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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
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Tue, 12/17/2024
December EQRS Stakeholder Meeting
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