FDASeptember 3, 2019device

Achilles Express Bone Sonometer

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

The hazard

Certain Achilles Express and Achilles Insight systems were shipped with European CEE-7/7 Type Power Cords to countries where three protruding pin plugs are required for protective earth connection.

What to do

FDA enforcement status: Terminated

Brands named

ge healthcare

UPCs

830331004004118303310002461183033000014510830330050007878303300456359983033005000579830330050028878303300500391783033000410110830330004153118303300419090983033005000938

Recall history

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

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