Class II

Medical Device Recall: IntelePACS - InteleConnect / TechPortal

INTELERAD MEDICAL SYSTEMS INCORPORATED · October 17, 2025

Reason for Recall

Software application that receives digital images and data to be communicated, processed, manipulated, enhanced, stored, displayed has a bug that could cause data loss in Relevant Clinical Info field when modifying studies through Case Editor in either Technologist Portal or Referring Physician Portal, which could result in loss of clinical information, which could impact clinical decision-making.

Distribution

US Nationwide distribution in the states of AZ, CT, AL, IL, WA, MD, NJ,CA, TN, IN, FL, NC.

States Affected

NATIONWIDE

Quantity Affected

19

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0723-2026

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 - InteleConnect / TechPortal | SafeCheck