MOSAIQ Oncology Information System — Class II medical device recall Z-2293-2016
Ongoing recall by Elekta, Inc., reported 2016-08-03, distributed nationwide. It is possible that a change to an Order Set will not be saved in the current open Care Plan. This can result
| Recall number | Z-2293-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Elekta, Inc., Atlanta, GA, United States |
| Recall initiated | 2016-07-15 |
| Classified | 2016-07-27 |
| Reported by FDA | 2016-08-03 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BH, BS, CA, CZ, DE, ES, GB, HU, SE, TR, ZA |
| Quantity | 383 |
Product
MOSAIQ Oncology Information System
Reason for recall
It is possible that a change to an Order Set will not be saved in the current open Care Plan. This can result in a wrong chemo dose in the order.
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-2293-2016. 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.