MOSAIQ Oncology Information System The product is used to manage… — Class II medical device recall Z-0731-2017
Terminated recall by Elekta, Inc., reported 2016-12-21, distributed nationwide. Edits to Particle field definition parameters may not be saved when the field definition window is saved.
| Recall number | Z-0731-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Elekta, Inc., Atlanta, GA, United States |
| Recall initiated | 2016-12-02 |
| Classified | 2016-12-09 |
| Reported by FDA | 2016-12-21 |
| Terminated | 2021-11-05 |
| Distributed | Nationwide (US) |
| Countries outside the US | GB, IT, JP, KR, SE |
| Quantity | 47 |
Product
MOSAIQ Oncology Information System The product is used to manage workflows for treatment planning and delivery. It supports information flow among healthcare facility personnel and can be use wherever radiotherapy and chemotherapy are prescribed.
Reason for recall
Edits to Particle field definition parameters may not be saved when the field definition window is saved.
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-0731-2017. 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.