Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
bk3000 Recalled by B-K Medical A/S Due to The internal power connections at the power inlet...
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
bk3000, model #2300-11; bk3500, model #2300-41; bk5000, model #2300-61; and bkActive 2300, model #2300-66, ultrasound system with battery option.
Quantity: 1648 devices
Why Was This Recalled?
The internal power connections at the power inlet of the ultrasound devices can come loose resulting in the potential for excessive heat which could lead to a thermal event or the device becoming inoperable.
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