Philips Provides Update on Sleep Care Product Recall
Philips Respironics has been conducting comprehensive testing to address potential health risks related to the PE-PUR sound abatement foam in the devices.
Read MoreDec 29, 2021 | Company News, Recalls | 0 |
Philips Respironics has been conducting comprehensive testing to address potential health risks related to the PE-PUR sound abatement foam in the devices.
Read MoreDec 21, 2021 | Equipment management, HTM Programs, Medical Equipment, Preventive Maintenance | 0 |
Having an optimized HTM program that delivers efficiency and effectiveness to a hospital is an often-overlooked part of the patient satisfaction equation.
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. Â
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