Medical device recalls Moderate risk

INTELERAD MEDICAL SYSTEMS INCORPORATED recalls IntelePACS - InteleConnect / TechPortal

Recall date
October 17, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0723-2026
FDA classification
Class II
Brand / firm
INTELERAD MEDICAL SYSTEMS INCORPORATED
Sold / distributed
US Nationwide distribution in the states of AZ, CT, AL, IL, WA, MD, NJ,CA, TN, IN, FL, NC.

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

IntelePACS - InteleConnect / TechPortal

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