FDA Device recall Z-2917-2018
MOSAIQ Oncology Information System
- FDA Device
- Class II
- terminated
- Published 2018-08-29
On 2018-08-29 the FDA classified a Class II recall of MOSAIQ Oncology Information System by Elekta, citing order Status Remains Approved When Should Indicate Complete.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2917-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-08-03 |
| Published | 2018-08-29 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Elekta |
| 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, WY |
Product
MOSAIQ Oncology Information System
Reason
Order Status Remains Approved When Should Indicate Complete.
Identifiers
| code_info | Software Build(s) 2.64 SP3 and higher |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2917-2018%22
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