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News You Need to Know Today
FDA clears blood clot removal system for PE | Catheters recalled | Tiny clot-busting robots | Stroke care keeps evolving
Friday, June 20, 2025
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Editor's Choice: Vascular & Endovascular

FDA clears blood clot removal system for treating pulmonary embolism

The Aventus Thrombectomy System was already cleared to treat blood clots in the peripheral arteries. This latest approval comes after positive results from an IDE study were published in JSCAI.

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Inquis Medical Aventus Thrombectomy System
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FDA clears blood clot removal system for treating pulmonary embolism

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Inquis Medical Aventus Thrombectomy System
The Aventus Thrombectomy System was already cleared to treat blood clots in the peripheral arteries. This latest approval comes after positive results from an IDE study were published in JSCAI.
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Angiographic catheters recalled due to safety risk

The new Class I recall includes nearly 27,000 devices that could potentially experience a harmful defect during use. 

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Cook Medical angiographic catheter recall
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Angiographic catheters recalled due to safety risk

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Cook Medical angiographic catheter recall
The new Class I recall includes nearly 27,000 devices that could potentially experience a harmful defect during use. 
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Marijuana use linked to blood vessel damage—impact seen with smoking and edibles

"As cannabis legalization increases, it is crucial to understand the public health and clinical implications of marijuana use," researchers wrote in JAMA Cardiology.

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cannabis weed marijuana heart health doctor cardiologist
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Marijuana use linked to blood vessel damage—impact seen with smoking and edibles

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cannabis weed marijuana heart health doctor cardiologist
"As cannabis legalization increases, it is crucial to understand the public health and clinical implications of marijuana use," researchers wrote in JAMA Cardiology.
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Tiny clot-busting robots could transform care for stroke and heart attack patients

The robots are capable of swimming through a patient’s vascular system and removing blood clots. “It’s unbelievable," one Stanford researcher said. "This is a sea-change technology that will drastically improve our ability to help people.”

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milli-spinner thrombectomy designed to target blood clots by engineers with Stanford University
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Tiny clot-busting robots could transform care for stroke and heart attack patients

Share on Twitter Share on Facebook Share on Linkedin
milli-spinner thrombectomy designed to target blood clots by engineers with Stanford University
The robots are capable of swimming through a patient’s vascular system and removing blood clots. “It’s unbelievable," one Stanford researcher said. "This is a sea-change technology that will drastically improve our ability to help people.”
READ MORE >

Stroke care continues to evolve thanks to AI, cardiologists and more

Gregg Fonarow, MD, discussed the American Heart Association's stroke guidelines, the growing influence of AI and much more.

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Video interview with Gregg Fonarow, MD, explaining the success of the AHA Get With The Guidelines-Stroke program, during AHA 2024.
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Stroke care continues to evolve thanks to AI, cardiologists and more

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Video interview with Gregg Fonarow, MD, explaining the success of the AHA Get With The Guidelines-Stroke program, during AHA 2024.
Gregg Fonarow, MD, discussed the American Heart Association's stroke guidelines, the growing influence of AI and much more.
READ MORE >

New-look peripheral stent with expandable spikes receives FDA’s de novo classification

California-based Reflow Medical gained the approval after submitting data from the DEEPER REVEAL clinical trial. The device was associated with a high success rate and improved outcomes in CLTI patients.

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Reflow Medical Spur Peripheral Retrievable Stent System. Reflow Medical, a California-based medtech company focused on cardiovascular disease treatments, has received the FDA’s de novo classification for its Spur Peripheral Retrievable Stent System. De novo classification represents an alternative pathway to gaining FDA approval when no comparable devices are currently available.
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New-look peripheral stent with expandable spikes receives FDA’s de novo classification

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Reflow Medical Spur Peripheral Retrievable Stent System. Reflow Medical, a California-based medtech company focused on cardiovascular disease treatments, has received the FDA’s de novo classification for its Spur Peripheral Retrievable Stent System. De novo classification represents an alternative pathway to gaining FDA approval when no comparable devices are currently available.
California-based Reflow Medical gained the approval after submitting data from the DEEPER REVEAL clinical trial. The device was associated with a high success rate and improved outcomes in CLTI patients.
READ MORE >

How anticoagulants may impact a patient’s risk of gastrointestinal bleeding after TAVR

Researchers tracked the rates of major gastrointestinal bleeding in patients with AFib randomized to receive edoxaban or a vitamin K antagonist after a successful TAVR procedure.

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heart drugs with stethoscope
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How anticoagulants may impact a patient’s risk of gastrointestinal bleeding after TAVR

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heart drugs with stethoscope
Researchers tracked the rates of major gastrointestinal bleeding in patients with AFib randomized to receive edoxaban or a vitamin K antagonist after a successful TAVR procedure.
READ MORE >

Terumo Interventional Systems launches dual-layer micromesh carotid stent after FDA approval

The dual-layer micromesh stent was designed with the flexibility of an open-cell stent and is available in multiple sizes.

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Roadsaver Carotid Stent System
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Terumo Interventional Systems launches dual-layer micromesh carotid stent after FDA approval

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Roadsaver Carotid Stent System
The dual-layer micromesh stent was designed with the flexibility of an open-cell stent and is available in multiple sizes.
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