HeartStart XL+ Defibrillator/Monitor, Model 861290
Class I - DangerousWhat Should You Do?
- Check if you have this product: All units manufactured prior to 1 May 2017.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Philips North America, LLC
- Reason for Recall:
- The rotary therapy selector switch may fail, resulting in unexpected device behavior. These behaviors include: The device may not turn on; The device may not perform the selected function; The device may deliver a shock with an energy level different from the setting selected by the user.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
HeartStart XL+ Defibrillator/Monitor, Model 861290
Product Codes/Lot Numbers:
All units manufactured prior to 1 May 2017.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0498-2020
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