FDASeptember 3, 2019device

Achilles Insight 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

830336036520098303360456499982433040028824330400378243307000882433120015824330800058243304003582433040039824331400208243329000582433130044

Recall history

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

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