FDA Alerts

Becton Dickinson CareFusion 303, Inc. Recalls Alaris System Pump Module and Pump Module Door Assembly Replacement Kits Due to the Potential for Stuck or Unresponsive Keys

Becton Dickinson (BD) CareFusion 303, Inc. Recalls Alaris System PC Unit and PC Unit Front Case Keypad Replacement Kits Due to Risk of Stuck or Unresponsive Keys

CME America Updates Recall of BodyGuard Infusion Pump System Due to Risk of Over-, and Under-Infusion

Verathon, Inc. Recalls GlideScope Core One TouchSmart Cable (OneTouch cable), Due to Partial or Complete Loss of Image During Use

CME America Recalls BodyGuard Infusion Pump System Due to Risk of Over-, and Under-infusion

Becton Dickinson (BD) CareFusion 303 Inc. Recalls Alaris System Infusion Pumps Due to Software and System Errors

Medtronic Recalls MiniMed Insulin Pumps for Incorrect Insulin Dosing

GE Healthcare Recalls Carestation 600 Series Anesthesia Systems Due to Loss of Mechanical Ventilation

GE Healthcare Recalls CARESCAPE Respiratory Modules Due to Incorrect Oxygen Values

Stryker Launches Voluntary Field Action for Specific Units of The LIFEPAK 15 Monitor/Defibrillator