Much of Medtronic’s work in diabetes this year has focused specifically on bringing new technologies to European patients—and its latest purchase continues this trend. The medtech giant snapped up the ...

The FDA has ordered a recall of Medtronic’s SynchroMed II implantable infusion pump, models 8637-20 and 8637-40, distributed between May 2004 and July 8, 2011, according to an FDA news release. The ...

DUBLIN, July 07, 2020 (GLOBE NEWSWIRE) -- Medtronic plc (NYSE:MDT), the global leader in medical technology, today introduced the MiniMed™ Mio™ Advance infusion set to all Medtronic insulin pump ...

September 13, 2011 — A class I recall has been issued for certain Medtronic implantable programmable infusion pumps (SynchroMed II), the US Food and Drug Administration (FDA) announced yesterday.

With a great deal of hype, and a few delays from the US Food and Drug Administration (FDA), Medtronic in September 2013 released its newest combined pump and continuous glucose monitor (CGM), the ...

The thin plastic tubing of infusion sets that connect insulin pumps to the body typically need to be changed every two or three days—but a new version in the U.S. more than doubles that timespan. The ...

Medtronic has issued an urgent medical device correction on its SynchroMed II implantable drug infusion pumps, warning that the batteries in certain devices might suddenly fail, according to a news ...

* Medtronic-‍determined a component, vent membrane, in recalled infusion sets may be susceptible to being blocked by fluid during process of priming/fill-tubing * Medtronic PLC - ‍recall is related to ...

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 ...

CHICAGO (Reuters) - Medtronic Inc has sent a letter to physicians warning about possible reduced battery performance in a small percentage of its SynchroMed II Implantable Drug Infusion Pumps, the ...

Medtronic, Inc., said Wednesday that eight deaths and 270 serious or life-threatening injuries that occurred between May 1996 and September 2010 were tied to an improperly working product that it ...