Medtronic is recalling specific lots of MiniMed infusion sets after learning of the risk of insulin overdelivery. The global, voluntary recall affects older insulin pump infusion sets that featured a ...

For the third time in the last two years, Baxter has been hit with the FDA’s most serious label for a recall affecting its infusion pump systems. This time around, the Class I recall notice is linked ...

The U.S. Food and Drug Administration has announced a new initiative to address safety problems associated with external infusion pumps, which are often used to deliver fluids, including nutrients and ...

The U.S. Food and Drug Administration on Wednesday gave Minnesota-made syringe infusion pumps a Class 1 recall classification, the most serious category of market withdrawals. The device is made by ...

Starting insulin pump therapy can feel like stepping into a new world but many have found going onto an insulin pump well worth the initial effort. This is a guide to starting insulin pump therapy, ...

When you get started on a pump, you should be given full training on how to use and get the most out of your new pump. This guide therefore serves as an introduction to what’s involved in using an ...

The NDA for SPN-830 is supported by data from an extensive development program that includes the phase 3 TOLEDO study and a supportive open-label study. The New Drug Application (NDA) for SPN-830 ...