1. Home
  2. Clinical Topics
  3. Cardio-Pulmonary
  4. FDA issues safety communication for HeartStart AEDs
Cardio-PulmonaryClinical TopicsDrugs and DevicesHealthcare & TechnologyNewsPatient SafetyWeb ExclusivesWorkplace Management

FDA issues safety communication for HeartStart AEDs

Share

On Nov. 25, the U.S. Food and Drug Administration (FDA) issued a safety communication stating that certain HeartStart automated external defibrillator (AED) devices made by Philips Medical Systems, a division of Philips Healthcare, may be unable to deliver needed defibrillator shock in a cardiac emergency situation. These devices were manufactured and distributed between 2005 and 2012 under the names HeartStart FRx, HeartStart HS1 Home, and HeartStart HS1 OnSite Read more.

Leave a Reply

Your email address will not be published.

Fill out this field
Fill out this field
Please enter a valid email address.

Get your free subscription to NurseLine!

NurseLine Newsletter

  • Hidden

*By submitting your e-mail, you are opting in to receiving information from Healthcom Media and Affiliates. The details, including your email address/mobile number, may be used to keep you informed about future products and services.

Recent Posts