Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
bk3000 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE HealthCare has become aware that the Instructions...
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 Ultrasound System w/battery; Model No. 2300-66; System, Imaging, Pulsed Doppler, Ultrasonic
Quantity: 496 units
Why Was This Recalled?
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life handling procedures, or general battery safety precautions.
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