# FDA recall Z-2917-2018

> **Elekta, Inc.** · Class II · device recall initiated 2018-08-03.

## Product

MOSAIQ Oncology Information System

## Reason for recall

Order Status Remains Approved When Should Indicate Complete.

## Distribution

AK, AZ, CA, CO, CT, DC, FL, GA, IA, ID, IL, KS, KY, LA, MA, MD, ME, MI, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, WA, WI, WV, and WY  Australia, Canada, Ireland, New Zealand, Portugal, Singapore, South Africa, Spain, Sweden, and United Kingdom

## Key facts

- **Recall number:** Z-2917-2018
- **Recalling firm:** Elekta, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-08-03
- **Report date:** 2018-08-29
- **Termination date:** 2024-09-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Atlanta, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2917-2018

## Citation

> AI Analytics. FDA recall Z-2917-2018. Retrieved 2026-07-10 from https://api.ai-analytics.org/recall/Z-2917-2018. Source: US FDA. Licensed CC0.

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