Class II

Medical Device Recall: IntelePACS (Image Fusion Module) - InteleViewer

INTELERAD MEDICAL SYSTEMS INCORPORATED · February 5, 2025

Reason for Recall

A software application that receives digital images and data from various sources has a bug in specific software versions that will calculate the Standard Uptake Value (SUV) incorrectly for PET/CT studies acquired on the days of Daylight Savings Time (DST); only on dates in which DST transition occurs; all other dates are unaffected. An incorrect SUV may lead to an incorrect diagnosis.

Distribution

Worldwide - US Nationwide distribution in the states of AZ, NC, MI, FL, NH, WY, CA, SC, AL, AR, IN, MD, CO, TN, IL, NJ, OH, MN, WV, KE, NE, VA, WA, GE, WI and the countries of New Zealand, Canada, Australia

States Affected

NATIONWIDE

Quantity Affected

88

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1208-2025

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.

INTELERAD MEDICAL SYSTEMS INCORPORATED Medical Device Recall: IntelePACS (Image Fusion Module) - InteleViewer | SafeCheck