Medtronic is warning of a potential safety risk involving its MiniMed insulin pumps that has led to at least one hospitalization and one death, according to the Star Tribune. Medtronic said its ...

Medtronic has recalled some of its insulin pumps after injuries and one death were reported due to the device malfunctioning, according to a US Food and Drug Administration announcement on Wednesday.

Medtronic MiniMed insulin pumps are being recalled due to an issue that can lead to incorrect dosing. The affected pumps include the MiniMed 630G and MiniMed 670G. The recall affects 322,055 devices.

SPRINGFIELD, Mo. — The Food and Drug Administration (FDA) has issued a class I recall on certain types of Medtronic insulin pumps. A class I recall means the devices could cause serious injuries or ...

The FDA announced that Medtronic expanded two recalls relating to the MiniMed 600 series of insulin pumps and MiniMed 508 remote controllers. Both were designated by the agency as Class I, the most ...

The FDA issued a warning to patients who use a particular insulin pump system that unauthorized people could access it and change how much insulin a patient receives. In the warning posted Sept. 20, ...

Medtronic is expanding a recall of its MiniMed insulin pumps after a broken retainer ring led patients to receive the incorrect dose of insulin. The recall, first announced in November 2019, was ...

A retrospective study of over 100 pediatric and adolescent patients showed that providing virtual training for insulin pump use was both safe and effective. Initiating insulin pumps virtually for ...

Medtronic has updated a previous recall of its MiniMed 600 series insulin pumps to include all with a potentially problematic clear retainer ring, not just those that appear damaged. The U.S. Food and ...