Infusion pumps released with incorrect software can experience unexpected performance problems, including issues with essential functions and risk measures.
 Kerendia (finérénone) est indiqué chez l'adulte dans le traitement de l'insuffisance cardiaque à fraction d'éjection légèrement réduite ou préservée (FEVG ≥ 40 %) afin de réduire le risque de décès d'origine cardiovasculaire ainsi que d'hospitalisation et de consultation en urgence pour cause d'insuffisance cardiaque. 
Nipro recalls bicarbonate dialysate concentrate due to contamination. Learn about potential serious injuries, fatality risks and essential steps for healthcare providers and patients for this Class I recall.
Sensorized Guidewire Issue from Centerline Biomedical
In May 2025, Medtronic issued a voluntary recall notification to global customers related to specific Newport™ HT70 and HT70 Plus ventilators and certain related Newport™ service parts. The FDA recently designated this voluntary action by Medtronic as a Class I recall. 
With this recall, Medtronic i
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