Infusion Pump FDA Alerts
FDA Alerts
CME America Recalls BodyGuard Infusion Pump System Due to Risk of Over-, and Under-infusion
Mon Mar 30 2020read article
FDA Alerts
Class 1 Recall: Medtronic Recalls SynchroMed II and SynchroMed EL Implantable Drug Infusion Pumps Due to Failure of Priming Bolus – Update Related to May 2013 Recall
Wed Mar 15 2017read article
FDA Alerts
Class 1 Recall: Medtronic SynchroMed II and SynchroMed EL Implantable Infusion Pump and Refill Kits
Fri Jan 14 2011read article