# FDA recall Z-0723-2026

> **INTELERAD MEDICAL SYSTEMS INCORPORATED** · Class II · device recall initiated 2025-10-17.

## Product

IntelePACS - InteleConnect / TechPortal

## 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.

## Key facts

- **Recall number:** Z-0723-2026
- **Recalling firm:** INTELERAD MEDICAL SYSTEMS INCORPORATED
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-10-17
- **Report date:** 2025-12-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Montreal, N/A, Canada

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0723-2026

## Citation

> AI Analytics. FDA recall Z-0723-2026. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0723-2026. Source: US FDA. Licensed CC0.

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