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 ...

Johnson & Johnson’s Abiomed has recalled automated controllers for its Impella heart pumps over a fault linked to three ...

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

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 ...

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

Medtronic announced a recall of all implantable cardioverter defibrillator and cardiac resynchronization therapy defibrillators manufactured after Oct. 13, 2017 with a glassed feedthrough.Due to ...

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 users who experience shortened battery life should contact their local support team to assess whether a replacement pump is needed. In 2021, Medtronic expanded the Class I recall of its ...

Medtronic recalls certain devices due to the possibility that the battery may deplete below its designed threshold. Baxter to recall some circuits and adapter assemblies used in ventilators. 9 Out ...

Customers are being notified of the importance of checking built-in alerts and alarms for battery status and to contact Medtronic for pump replacement if affected by this issue. GALWAY, Ireland ...