FDANovember 30, 2023device

bkActiv Ultrasound System 2300, Model numbers 2300-56 and 2300-66.

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

The hazard

An issue on the Dual Live Compare feature on the bkActiv system could result in a measurement error.

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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bkActiv Ultrasound System 2300, Model numbers 2300-56 and 2300-66. — Recall Details · AllClear