The FDA is amplifying a recall from Medtronic for its acid reflux testing system, after the company said it received 33 reports of serious injuries related to the device. The Bravo capsule-based ...

Medtronic has recalled Bravo capsule delivery devices due to product malfunctions that have been tied to 33 serious injuries, according to an early alert published Tuesday by the Food and Drug ...

Used for diagnosing gastroesophageal reflux, the devices may not attach or detach correctly, potentially causing serious ...

Medtronic's growth strategies, dividend stability, and innovation focus amidst debt concerns and market risks. Click here to ...

Medline has expanded a correction involving procedure kits containing its Medtronic aortic root cannulas, due to risk of serious injury or death. The expanded recall comes after Medline confirmed ...

Medical device recalls are essential to patient safety, addressing critical issues in devices that may pose health risks. Here are some of the most recent recalls reported to the FDA: Zoll recalls ...

The next generation of deep-brain stimulation automatically corrects the precise brain waves that create symptoms of ...

The tennis pro is teaming up with the medical device giant to launch a global campaign aimed at inspiring people living with type 1 diabetes.

Born with a severe heart defect, Kendreya’s condition worsened until a team of doctors and donors made surgery possible.

According to a new listing at the FDA device recalls and alerts webpage, Dublin-based Medtronic plc., requested customers quarantine any Bravo CF capsules, an esophageal pH monitoring system.

Despite these factors, Meyer touted the study's large sample size, and said its prospective design reduced the risk of recall bias. He added that lifestyle ... Hospira, Janssen, Medtronic, MSD, Pfizer ...

Merit announces preliminary unaudited revenue for the quarter ended June 30, 2025 ...