# FDA recall Z-0941-2026

> **DICOM Grid, Inc.** · Class II · device recall initiated 2025-11-18.

## Product

Intelerad InteleShare software, with ProViewer component

## Reason for recall

Software intended to aid in diagnosing conditions, planning treatments, visualizing anatomical structures has a bug that, if all of following are met: Viewing images in InteleShare viewer; Multiplanar reconstruction applied; Manual rotation applied, could result in inaccurate length measurement tool values that could compromise diagnostic accuracy, lead to misdiagnosis or inappropriate follow-up.

## Distribution

US: AZ, TX, GA, NV, MO, MI, IL, OH, CT, OR, FL, NY, NM, MN, PA, AK, ND, NJ, VA, WA, NC, TN, WI, GA, AK, CA, SD, CO, MA, WV, MN, KS, MD, VT, IA, RI, AL, ID, LA, PR, NH, IN, OK, UT, NE, SC, AR, DE  OUS: CA, NZ, AU, GB, BE, FR, IT, NO, SE

## Key facts

- **Recall number:** Z-0941-2026
- **Recalling firm:** DICOM Grid, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-11-18
- **Report date:** 2025-12-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Raleigh, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0941-2026

## Citation

> AI Analytics. FDA recall Z-0941-2026. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0941-2026. Source: US FDA. Licensed CC0.

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