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FDAMarch 14, 2025device

Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038

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

The hazard

A potential weakness has been identified in the probe body, so that, in a specific production batch, liquid may leak from the terminal part of the casing near the cable.

What to do

FDA enforcement status: Completed

Brands named

esaote s p aesaote

UPCs

0805604453891

Recall history

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

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