FDASeptember 4, 2024device

bk3000, model #2300-11; bk3500, model #2300-41; bk5000, model #2300-61; and bkActive 2300, model #2300-66, ultrasound system with battery option.

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

The hazard

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.

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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