FDAFebruary 27, 2026device

SIGNA Premier systems

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

The hazard

Whole-Body MR scanners used to produce images of the inside of the human body to aid diagnosis of disease may have been manufactured/serviced with ferrous (steel) fittings instead of non-ferrous (brass) fittings on the magnet rear and if system is accessed to perform service while the magnet is ramped, the magnetic field could attract the ferrous fittings potentially resulting in personnel injury.

What to do

FDA enforcement status: Ongoing

Brands named

ge healthcare

UPCs

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Recall history

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

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