MOSAIQ Oncology Information System — Class II medical device recall Z-2052-2016
Terminated recall by Elekta, Inc., reported 2016-07-06, distributed in AK, AZ, CA, FL, GA, IL, IN, LA…. It is possible that that the selected Plan-of-the Day could be accidently changed by scrolling the mouse wheel
| Recall number | Z-2052-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Elekta, Inc., Atlanta, GA, United States |
| Recall initiated | 2016-06-17 |
| Classified | 2016-06-27 |
| Reported by FDA | 2016-07-06 |
| Terminated | 2020-08-18 |
| Distributed | AK, AZ, CA, FL, GA, IL, IN, LA, MD, MI, MO, NJ, NY, OH, OR, PA, PR, TN, TX, UT, VA, WA |
| Countries outside the US | CA, DE, DK, FI, GB, IL, JP, NL, NO, SE |
| Quantity | 69 |
Product
MOSAIQ Oncology Information System
Reason for recall
It is possible that that the selected Plan-of-the Day could be accidently changed by scrolling the mouse wheel up and down and inadvertently selecting another plan.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2052-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.