FDA tags Sentec/Percussionaire’s breathing circuit recall as Class I
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medtechdive5d
FDA labels recall of discontinued Olympus endoscope part as Class I
The update comes about six weeks after an early alert flagged reports of 120 injuries and one death linked to reprocessing of ...
FierceBiotech1d
FDA amplifies BD atherectomy safety alert following 4 deaths
The FDA is getting the word out on a high-risk issue related to artery-clearing catheters from BD’s Bard Peripheral Vascular ...
2025 Medical Device Cybersecurity Trends: What Will Shape The Industry?
What will the industry face or achieve in 2025? These trends will be critical in medical device cybersecurity.
FDA Approval Race: AI-Powered Innovations Reshape the Healthcare Landscape
Beyond Stargate's big players, a growing number of innovators have been revolutionizing healthcare by making recent ...
MassDevice4d
Medline has a Class I arterial catheter recall
The FDA labeled a recall of integrated arterial catheters made by Medline Class I, the most serious kind of recall.
JD Supra8d
How New Executive Orders May Affect FDA’s Medical Device Operations
Several executive orders recently signed by US President Donald Trump may have significant implications for the US Food and Drug Administration ...
Yahoo Finance8d
FDA labels recall of discontinued Olympus endoscope accessory as Class I
In recent years, Olympus has recalled other devices because of patient safety risks and ... In its Class I recall notice, the agency’s most serious classification, the FDA said patient exposure to a ...
FDA approved the first new kind of pain medication in 27 years. Here’s how it works
The FDA just approved a new type of pain medication, and it's a non-opioid called suzetrigine that stops body pain at its ...
Fox Business on MSN11d
Elizabeth Warren grilled RFK Jr on drug company money, but received over $5M from health industry
Mass., grilled Robert F. Kennedy Jr. over his plans to profit off of drug companies or lawsuits after being Health and Human ...
Healio10d
FDA recalls Mercury Medical T-piece resuscitator due to ventilation control component
The FDA has recalled Mercury Medical’s Neo-Tee T-Piece Resuscitator, a gas powered resuscitator intended primarily for ...