Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Avalon Ultrasound Transducer. Directs low-energy ultrasound beam toward the fetal Recalled by Philips North America Llc Due to Potential for inaccurate fetal heart rate measurements when...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips North America Llc directly.
Affected Products
Avalon Ultrasound Transducer. Directs low-energy ultrasound beam toward the fetal heart and externally monitors fetal heart rate.
Quantity: 6,915 units
Why Was This Recalled?
Potential for inaccurate fetal heart rate measurements when monitoring multiples.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips North America Llc
Philips North America Llc has 301 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report