The Food and Drug Administration published an early alert for the recall on Tuesday. No deaths have been associated with the ...

The FDA announced a recall of certain Medtronic Bravo esophageal pH monitoring capsules, which help in diagnosing ...

The FDA issued a notice identifying a high-risk device issue associated with a Medtronic recall of Bravo CF capsule delivery ...

The FDA is amplifying a recall from Medtronic for its acid reflux testing system, after the company said it received 33 ...

Medtronic, with fiscal 2022 sales of $31.7 billion, is the largest medical device manufacturer in the industry, which puts it at higher recall risk because it simply makes more products than ...

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 more ...

Medtronic recalls aneurysm-treating device linked to four deaths. The FDA recall affects more than 25,000 of the Fridley-run company’s devices and follows reports of 17 injuries.

Medtronic has reported 28 incidents, 22 injuries, and no deaths for this issue. The recall impacts around 350k devices distributed between Oct. 13, 2017-June 9, 2023.

Thursday, Medtronic Plc (NYSE:MDT) said it is recalling certain devices and updating use instructions for another due to the possibility that the battery may deplete below its designed threshold.

In May 2025, Medtronic issued a voluntary recall notification to global customers related to specific Newport™ HT70 and HT70 Plus ventilators and certain related Newport™ service parts. The ...

Medtronic Plc announced a voluntary recall Friday of certain insulin pumps after customers said a single drop, bump, or physical impact could shorten their battery life. The Galway, Ireland-based ...

In May 2025, Medtronic issued a voluntary recall notification to global customers related to specific Newport™ HT70 and HT70 Plus ventilators and certain related Newport™ service parts. The ...