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

• Philips Respironics Issues Voluntary Recall Notification/Field Safety Notice* for the V60 Ventilator Product Family

• Philips Respironics CPAP, BiPAP, and Ventilator Recalls: Frequently Asked Questions

• Counterfeit At-Home OTC COVID-19 Diagnostic Tests

• Potential for Internal Pump Malfunction in the Medtronic HVAD

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