Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SIGNA Architect nuclear magnetic resonance imaging system Recalled by GE Healthcare, LLC Due to Under certain conditions, some slices may be missing...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact GE Healthcare, LLC directly.
Affected Products
SIGNA Architect nuclear magnetic resonance imaging system
Quantity: 2 devices
Why Was This Recalled?
Under certain conditions, some slices may be missing which can lead to a gap of anatomy in the 3D Volume images.
Where Was This Sold?
This product was distributed to 18 states: AZ, CA, FL, GA, IL, LA, MD, MA, MN, NH, NJ, NY, NC, OH, OK, TX, VA, WA
About GE Healthcare, LLC
GE Healthcare, LLC has 474 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report