Please provide your email address to receive an email when new articles are posted on . The FDA has designated a recall of a sheath used to introduce and/or guide the placement of interventional and ...

Yesterday the US Food and Drug Administration (FDA) announced a Class I recall for the low-profile, thin-walled peripheral guiding sheath known as Halo One. Device manufacturer Bard Peripheral ...

- Radial access remains one of the fastest-growing cardiac cath lab practice trends in the U.S. MINNEAPOLIS, Jan. 25, 2016 (GLOBE NEWSWIRE) -- Vascular Solutions, Inc. (Nasdaq:VASC) today announced ...

PEMBROKE PINES, Fla., Aug. 2, 2023 /PRNewswire/ -- EOSolutions Corp., a trailblazing medical technology company committed to innovation, is delighted to announce the 510k submission, through a Design ...

Bard Peripheral Vascular issued a voluntary recall of its Halo One Thin-Walled Guiding Sheath over structural issues with the device, according to a Food and Drug Administration report. The sheath is ...

Use of a balloon-expandable large-bore sheath during transfemoral transcatheter aortic valve replacement demonstrated similar rates of mortality, vascular complications and bleeding compared with a ...

Use of a novel inflatable sheath that eases transfemoral access appears feasible and safe, making the approach available to many patients with PAD, reports a small study published online January 30, ...

BRIDGEWATER, N.J.--(BUSINESS WIRE)-- Results from a Cordis analysis presented at the 14 th Annual International Society for Pharmacoeconomics and Outcomes Research (ISPOR) congress in Madrid indicates ...

PALO ALTO, Calif.--(BUSINESS WIRE)--Vascular Closure Systems, Inc.: The Company is pleased to announce the successful conclusion of Phase I and Phase II of the First in Human (FIH) clinical trial for ...

Transcatheter aortic valve replacement (TAVR) can be made more user-friendly by placing both arterial sheaths on the same side of the body, according to a center that has made unilateral access the ...