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FDA issues early alert for Baxter’s Spectrum infusion pumpThe US Food and Drug Administration (FDA) has issued an early alert over a ‘potentially high-risk’ issue with certain Baxter ...
Members of the House of Representatives and the Senate have re-introduced legislation that would create a complete home ...
The FDA today issued a notice warning of a potential high-risk issue with certain Baxter Spectrum infusion pump systems.
Under federal law, device makers must submit adverse event reports they receive from patients to the FDA’s Manufacturer And User Facility Device Experience (MAUDE) database within 30 days, researchers ...
Baxter Healthcare has issued a recall for some Spectrum infusion pumps due to a potential defect involving missing motor mounting screws, which could lead to interruptions, delays or incorrect dosing ...
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Hepatic artery infusion pump therapy for colorectal liver metastasesDr. Katherine Poruk, a surgical oncologist at Mayo Clinic, says a specialized therapy known as hepatic artery infusion pump (HAIP) chemotherapy is an option for some. HAIP therapy targets tumors ...
The "North America and Europe Intravenous Infusion Pumps Market Size, Share & Trends Analysis Report by Product (Volumetric Infusion Pumps, Syringe Infusion Pumps), Disease Indication (Chemotherapy), ...
The provincial cancer agency is halting its use of an infusion pump line, due to concerns over leakage and heightened risk of ...
Developed in 2010, the Regenstrief National Center for Medical Device Informatics (REMEDI) is a flagship software solution that collects infusion pump data from a broad range of manufacturers. REMEDI ...
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