Medical Device Network on MSN13d
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 ...
The FDA today issued a notice warning of a potential high-risk issue with certain Baxter Spectrum infusion pump systems.
Members of the House of Representatives and the Senate have re-introduced legislation that would create a complete home ...
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 ...
The Food and Drug Administration March 5 announced that Baxter Healthcare Corporation recalled its Spectrum infusion pumps ...
SaaS unicorn Fractal has announced a strategic investment of $20 Mn in its in-house AI-driven supply chain management ...
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 MSN6d
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 ...
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