General FDA Alerts
CME America Recalls BodyGuard Infusion Pump System Due to Risk of Over-, and Under-infusion
GE Healthcare Recalls Giraffe Incubators and OmniBeds Due to Potential for Infants to Fall
Class 1 Recall: GE Healthcare Recalls CareScape R860 Inspiratory Safety Guard Due to Risk of Disconnection from Breathing Circuit
Class 2 Recall: Terumo Recalls Sarns" TCM and TCM II Cooling and Heating Systems and HX2" Temperature Management Systems Due to Revised Cleaning Instructions
Class 1 Recall: Vyaire Medical Recalls AirLife Humidification Chamber & Heated Breathing Circuit Kits Due to Manufacturing Error
Class 1 Recall: Zimmer Biomet Recalls Implantable Spinal Fusion Stimulators Due to Potential of Harmful Chemicals Which May Be Toxic to Tissues and Organs
Class 1 Recall: Magellan Diagnostics Inc. Recalls LeadCare Plus and Ultra Testing Systems Due to Inaccurate Test Results
Class 1 Recall: Abbott Vascular Recalls Coronary Catheters Due to Risks Stemming from Difficulty Removing Balloon Sheath
Class 1 Recall: Abbott-Thoratec Recalls HeartMate II LVAS Pocket System Controller Due to Risk of Patient Injury and/or Death during Backup Controller Exchange
Class 1 Recall: ReFlow Recalls Wingman 35 Crossing Catheters due to Tip Separation