Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Viterion TeleHealth Monitor Model Number V500 Recalled by Viterion TeleHealthcare Llc Due to Viterion telehealth monitors do not transmit "HI" (above...
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 Viterion TeleHealthcare Llc directly.
Affected Products
Viterion TeleHealth Monitor Model Number V500; Product Codes 08832984 (US) and 02080468 (UK) - Physiological patient monitor (without arrhythmia detection or alarms). Viterion V100, V100-BGM and V500 Telehealth Monitors transfer medical information.
Quantity: Domestic - 296 units, Foreign - 73 units
Why Was This Recalled?
Viterion telehealth monitors do not transmit "HI" (above the meter's measurable range) and "LO" (below the meter's measurable range) blood glucose readings from Bayer's Contour Elite XL blood glucose meters, or from Roche's Accu-Chek Advantage 03 and 04 meters to healthcare professionals.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Viterion TeleHealthcare Llc
Viterion TeleHealthcare Llc has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report