GE HealthCare Recalls Certain Carestation Devices Over Ventilation Risk
The Carestation anesthesia systems are being recalled due to a risk of ineffective ventilation in volume control mode, which could lead to serious injury or death.
The Carestation anesthesia systems are being recalled due to a risk of ineffective ventilation in volume control mode, which could lead to serious injury or death.
Philips has updated instructions for several ventilators to address aerosol deposits on internal sensors when used with in-line nebulizers.
Hamilton Medical issued a software correction for the Hamilton-C6 ventilator due to a failure to restart ventilation in sensor fail mode.
The Carestation anesthesia systems are being recalled due to a risk of ineffective ventilation in volume control mode, which could lead to serious injury or death.
SonarMed Airway acoustic sensors were recalled for a restricted inner diameter, causing compatibility issues with suction catheters.
Read MoreFresenius Kabi is recalling their Ivenix Infusion System LVP software due to serious anomalies that could harm patients, necessitating an urgent update to version 5.9.1.
Read MoreSmiths Medical is recalling its paraPAC Plus 300 and 310 Ventilator Kits due to a malfunction where the device may not cycle properly.
Read MoreAbbott is recalling its HeartMate II and 3 LVAS due to Extrinsic Outflow Graft Obstruction, which can lead to severe health risks or death.
Read MoreA consent decree of permanent injunction was issued against Philips Respironics, halting production of their sleep therapy devices.
Read MoreTeleflex is recalling the Arrow QuickFlash Radial Artery and Radial Artery/Arterial Line Catheterization Kits after reports of issues.
Read MoreVyaire Medical is recalling certain AirLife Manual Resuscitators due to a life-threatening manufacturing defect.