FDAOctober 9, 2025device

1202 Flex Focus Ultrasound System, cart models UA1214 and UA1814, used with: Flex Focus 200, Flex Focus 300, Flex Focus 400, Flex Focus 500, Flex Focus 700, Flex Focus 800; 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

05704916001056

Recall history

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

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1202 Flex Focus Ultrasound System, cart models UA1214 and UA1814, used with: Flex Focus 200, Flex Focus 300, Flex Focus 400, Flex Focus 500, Flex Focus 700, Flex Focus 800; System, Imaging, Pulsed Doppler, Ultrasonic — Recall Details · AllClear