Philips Recalls Panorama 1.0T HFO MRI System for Explosion Risk
Philips is recalling the Panorama 1.0T HFO due to risk of explosion during a quench procedure caused by excessive pressure buildup.
Read MorePhilips is recalling the Panorama 1.0T HFO due to risk of explosion during a quench procedure caused by excessive pressure buildup.
Read MoreSenators Durbin and Blumenthal have requested the Government Accountability Office (GAO) to review the FDA’s policies on medical device recalls, citing the Philips Respironics case and a significant increase in recalls.
Read MoreDespite a 115% increase in FDA recalls since 2018, MasterControl found that medical devices only contributed 4% of the total number.
Read MoreGetinge is recalling the Cardiohelp Emergency Drive due to a possible impairment of the ability of the emergency drive to be cranked.
Read MoreBecton Dickinson is recalling their Alaris Infusion Pumps due to compatibility issues with Cardinal Health Monoject syringes.
Read More