MOSAIQ — Class II medical device recall Z-1800-2014
Terminated recall by Elekta, Inc., reported 2014-06-25, distributed nationwide. When using CMA, if the user hovers the mouse pointer exactly above the direction dropdowns and then uses the m
| Recall number | Z-1800-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Elekta, Inc., Atlanta, GA, United States |
| Recall initiated | 2014-05-23 |
| Classified | 2014-06-16 |
| Reported by FDA | 2014-06-25 |
| Terminated | 2021-07-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, AT, AU, BD, BE, BG, BH, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DK, DZ, EC, EE, EG, ES, FI, FR, GB, GH, GR, HN, HR, HU, IE, IL, IN, IQ, IR, IT, JO, JP, LT, MA, MT, MX, MY, NL, NO, NZ, PA, PE, PK, PL, PT, RO, RS, RU, SA, SE, SI, SK, TH, TR, TW, UA, VE, ZA |
| Quantity | 723 |
Product
MOSAIQ, an oncology information system used to manage workflows for treatment planning and delivery. It supports information flow among healthcare facility personnel and can be used wherever radiotherapy and/or chemotherapy are prescribed.
Reason for recall
When using CMA, if the user hovers the mouse pointer exactly above the direction dropdowns and then uses the mouse thumbwheel or touchpad scroll bar, the direction selection might change when the intention was only to move the mouse to a different area of the screen.
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-1800-2014. 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.