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

• V60 and V60 Plus Ventilators Equipped with High Flow Therapy Software Versions 3.00 and 3.10 by Philips Respironics: Class I Recall - Due to Risk of Receiving Reduced Oxygen 

• BD Alaris System Software by BD: BD to Begin Remediation - Because Infusion Pump May Not Operate as Expected

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