FDAOctober 9, 2025device

bk3500 Ultrasound System w/battery; Model No. 2300-41; System, Imaging, Pulsed Doppler, Ultrasonic

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

b k medical a s

UPCs

05704916000264

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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