Medtronic Receives FDA Warning Letter for Insulin Pump Recall
The warning letter from the FDA is related to recalls of the MiniMed 600 series insulin infusion pump, and a device for MiniMed 508 and Paradigm pumps.
Read MoreDec 15, 2021 | Patient Care Equipment, Recalls | 0 |
The warning letter from the FDA is related to recalls of the MiniMed 600 series insulin infusion pump, and a device for MiniMed 508 and Paradigm pumps.
Read MoreDec 14, 2021 | Medical Equipment | 0 |
The acquisition and use of data is a hot topic in many circles, including healthcare. While concerns around the control and privacy of personal information dominate headlines, there is an upside to advancing data and analytics for businesses and supply chains. Learn about it here.
Read MoreDec 14, 2021 | Recalls, Ventilators | 0 |
The U.S. FDA has revealed that Medtronic’s recall of certain Puritan Bennett ventilators is Class 1—which means that using the devices could result in serious patient harm or even death.
Read MoreDec 13, 2021 | Recalls, Ventilators | 0 |
Philips and U.S. regulators are continuing discussions on an earlier recall of its ventilators, where parts being used contained potentially hazardous foam.
Read MoreDec 9, 2021 | Market Trends | 0 |
In this expert panel, four of the top luminaries in healthcare technology management discuss lessons learned from 2021 and what to expect in 2022 and beyond.
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