FDA Device recall Z-2293-2016
MOSAIQ Oncology Information System
- FDA Device
- Class II
- ongoing
- Published 2016-08-03
On 2016-08-03 the FDA classified a Class II recall of MOSAIQ Oncology Information System by Elekta, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2293-2016 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2016-07-15 |
| Published | 2016-08-03 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Elekta |
| Distribution | US |
Product
MOSAIQ Oncology Information System
Reason
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.
Identifiers
| code_info | Versions 2.50.05 and higher |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2293-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.