Those who rely on certain Medtronic MiniMed insulin pump models to administer insulin could be at risk, according to the U.S. Food and Drug Administration. On June 27, the FDA issued a recall on 11 ...

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.

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 ...

This Aug. 2, 2018, file photo shows the U.S. Food and Drug Administration building behind FDA logos at a bus stop on the agency's campus in Silver Spring, Md. AP Photo/Jacquelyn Martin, File SILVER ...

The US Food and Drug Administration issued a warning on Thursday about possible risk of hacking for some diabetes patients' insulin pumps. Certain insulin pumps from Medtronic MiniMed have been ...

The U.S. Food and Drug Administration is reminding patients who use the popular 600-series MiniMed insulin pumps made by Medtronic that the devices contain an issue that could cause their buttons to ...

The FDA reported two class I recalls associated with insulin pumps made by Dublin-based Medtronic plc, albeit for two significantly different issues. The two recalls affect roughly 495,000 units ...