Reported Apr 8, 2026 · Ongoing
SIGNA Premier systems
GE Healthcare LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: GE Healthcare LLC · 3001 W Radio Dr · Florence, SC · 29501-7806
Is this the product you have?
- SIGNA Premier systems
- Lot codes and dates
- UDI-DI/GTIN
0084068213526900195278010797
- System ID
415353UMR2415723SHMR19413253MR3T908725MR609652MR3TM488237168453T513584MR5513636EASTMR513636T1MR605333MRPRM832522CRMR1703858PRE2804675VA3T082427110162082427220143082427020147082427200242082427160461082427250139082427140382M4216469353745MR01GON5655515KRMR56474971KRMR56203791KRMR55433661KRMR56344161KRMR55774051KRMR55914661NOMRI2683332115974045GON1882380ESMRI27056983ESMRI26960129A203MR06690120MR0111524261VNMRI26792525VNMRI26592248VNMRI26809677
- UDI-DI/GTIN
- Amount recalled
- 41
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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