U.S. health officials have issued warnings on two separate Boston Scientific heart devices recently linked to injuries and ...

While neither warning is classified as a recall, the FDA has provided additional information for the two products. Boston Scientific told customers that its Endotak Reliance defibrillation leads with ...

The FDA is reviewing Boston Scientific's defibrillator leads after reports of rising shock impedance and 16 related deaths.

Boston Scientific has updated the instructions for use for products deployed in the implantation of its Watchman heart device ...

Boston Scientific is recommending updates to the instructions for use to minimize the issue, which has been tied to 17 deaths ...

Boston Scientific reported Q2 2025 sales of over $5bn, a 22.8% rise on Q2 2024, besting previous growth estimates of 19.5% at the high end.

The FDA has issued an early communication to warn of updated instructions for use for certain Boston Scientific Watchman access systems.

A company spokesperson said in a statement to MedTech Dive that direct causation between the deaths and calcification of the ...

--Boston Scientific Corporation today announced it has received U.S. Food and Drug Administration approval for the AGENT™ Drug-Coated Balloon, which is indicated to treat coronary in-stent ...

Boston Scientific Corp. BSX is making progress on efforts to resolve a corporate warning letter from the U.S. Food and Drug Administration, but doesn't see the warning letter being lifted by year ...