A51

HealthCare Alerts

Class 2 Device Recall AccuChek
Aurobindo Pharma USA, Inc. Issues Voluntary Nationwide Recall of Mirtazapine Tablets Lot Number 03119002A3 Due to Label Error on Declared Strength
LivaNova Recalls VNS Therapy SenTiva Generator Due to Reset Error
Smiths Medical ASD, Inc. Recalls Medfusion® 4000 Syringe Pumps Due to Malfunctioning Alarms and Potential Interruption of Therapy
Arrow EZ-IO intraosseous vascular access needle sets – risk of needle stick injury
ApexPro telemetry server – risk of loss of alarms for ECG and pulse oximetry monitoring (MDA/2019/045)
GE Healthcare Recalls Giraffe Incubators and OmniBeds Due to Potential for Infants to Fall
Cook Medical Recalls CrossCath® Support Catheters Due to a Manufacturing Error Which May Cause the Marker Bands to Dislodge or Cause Buckling
Class 2 Device Recall Homocysteine Enzymatic Assay
Medtronic Recalls SynchroMed II Implantable Drug Infusion Pump Due to the Potential Presence of Foreign Particles Inside the Pump Motor Assembly Which May Lead to a Pump Motor Stall

Events