FDA Device recall Z-2406-2026
MOSAIQ Oncology Information System
- FDA Device
- Class II
- ongoing
- Published 2026-06-17
On 2026-06-17 the FDA classified a Class II recall of MOSAIQ Oncology Information System by Elekta, citing software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2406-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-05-21 |
| Published | 2026-06-17 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Elekta |
| Distribution | US |
Product
MOSAIQ Oncology Information System
Reason
Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.
Identifiers
| code_info | Software Version: MOSAIQ 3.2/UDI: 07340201500071 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2406-2026%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.