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 ...

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

FDA highlights risks from recalled Medtronic devices tied to esophageal injuries and faulty cannulas, with serious health ...

Relating to certain of Medtronic’s Newport ventilator range, users have been advised to remove the affected units from ...

The recall comes more than one year after Medtronic announced it would exit the ventilator market.

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 ...

The U.S. Food and Drug Administration (FDA) has announced an expansion of an earlier Medtronic recall, now issuing a new Class 1 recall for Medline Industries' procedure kits that contain Medtronic ...

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 ...

Medtronic recalls thousands of implantable defibrillators that may deliver less-powerful shocks By Andrea Park Jul 19, 2023 10:35am Medtronic Class I recall implantable defibrillators implant ...

Medtronic Plc (NYSE:MDT) has initiated a recall for some versions of its StealthStation S8 application. The FDA deemed software recall as Class I, the most serious kind. The medical device giant ...