Class II
Medical Device Recall: OEC 3D
GE Medical Systems, LLC · March 21, 2025
Reason for Recall
OEC Elite and OEC 3D Mobile C-Arms Exceeding 4% Source to Image Distance in X-ray Field.
Distribution
US and OUS
Quantity Affected
Total for both products: 3472 (2,919 US; 553 OUS)
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1820-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.