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

Medtronic today announced that it issued a voluntary recall notification related to specific Newport ventilators and related ...

The company has asked users to monitor patients frequently to ensure the appropriate infusion is being delivered.

Fewer medical devices were recalled during the first three months of the year, following a surge in recalls in 2024. In the first quarter of 2025, there were 708 medical device recalls ...

Bengaluru: The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most serious", following reports of the deaths of four patients. The use of ...

The agency identified the recall as the most serious type. MDT’s Pipeline Vantage 027 devices are used to treat intracranial aneurysms. According to the FDA, the company has issued an urgent ...

March 18 (Reuters) - The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's (MDT.N), opens new tab embolization device as "most serious", following reports of the ...

Medical device recall events in 2024 reached their highest level since 2020 and more than 10% of them involved the most serious type of recall. There were 1,048 medical device recalls in 2024 ...

The devices are being recalled due to an increased risk for permanently entering Safety Mode. HealthDay News — Boston Scientific has issued a recall of Accolade pacemaker devices, according to a ...

Boston Scientific has issued a recall of Accolade pacemaker devices, according to a safety communication from the U.S. Food and Drug Administration. The Accolade devices under recall include the ...

Med-tech firms have gnashed their teeth for decades over the use of the term “recall,” given that some recalls are mere corrections to product labels while others entail a full product withdrawal. The ...