Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
bkActiv Ultrasound System 2300 Recalled by B-K Medical A/S Due to An issue on the Dual Live Compare feature...
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 B-K Medical A/S directly.
Affected Products
bkActiv Ultrasound System 2300, Model numbers 2300-56 and 2300-66.
Quantity: N/A
Why Was This Recalled?
An issue on the Dual Live Compare feature on the bkActiv system could result in a measurement error.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About B-K Medical A/S
B-K Medical A/S has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report