The following is a listing of recent U.S. Food and Drug Administration updates and activities:

• GE HealthCare Recalls TruSignal SpO2 Sensors for Issues That May Reduce Defibrillation Energy, Expose Patients to Unintended Voltage, or Give Inaccurate Readings

• Abiomed Recalls All Impella Left Sided Blood Pumps for Risk of Motor Damage After Contact with Transcatheter Aortic Valve Replacement (TAVR) Stent

• Medtronic Recalls Implantable Cardioverter Defibrillators (ICDs) and Cardi…

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