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Medium risk Drugs & MedicationsClass II

GE Healthcare LLC Recall

SIGNA Premier systems

Updated February 27, 2026

GE Healthcare LLC is recalling SIGNA Premier systems. 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.

Is the GE Healthcare LLC recalled? Yes. This product was recalled by FDA on February 27, 2026. Details below.

What is recalled

SIGNA Premier systems

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

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.

Brands affected

GE Healthcare LLC
Source
FDA
Category
Drugs & Medications
Recall ID
fda-Z-1767-2026
Classification
Class II
Recalled
February 27, 2026
Read the official notice

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