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 ...

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

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

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

Medtronic's operational headquarters are in Minneapolis, Minnesota. ·MedTech Dive·Courtesy of Medtronic Nick Paul Taylor Thu, Jun 12, 2025, 6:00 AM2 min read ...

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 ...

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

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

The firm will continue working directly with the FDA and other regulatory bodies around the world on the recall. Medtronic in February 2024 had announced its decision to exit its ventilator ...

The company began the recall after receiving four field complaints about tip separation before and during use.