"Baxter Healthcare recalls Spectrum infusion pumps due to potential defect, leading to medication dosing issues. FDA ...
Medical Device Network on MSN12d
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 ...
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 ...
Members of the House of Representatives and the Senate have re-introduced legislation that would create a complete home ...
Manitoba's cancer authority has stopped using an infusion pump line — made by a company whose IV pumps have been the subject ...
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 ...
MUMBAI: RBI is set to infuse nearly Rs 1.9 lakh crore into the banking system to address liquidity constraints, which have ...
Medical Device Network on MSN5d
Nearly a third of FDA medical device adverse event reports filed lateA study has found that nearly a third of medical device AEs were reported by manufacturers later than FDA's required 30-day ...
InfuSystem Holdings, Inc.’s INFU share price has dipped by 10.88%, which has investors questioning if this is right time to ...
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