Elekta Impac Software MOSAIQ, oncology information system - Product Usage: MOSAIQ is an oncology information system used to manage workflows for treatment planning and delivery. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MOSAIQ, oncology information system - Product Usage: MOSAIQ is an oncology information system used to manage workflows for treatment planning and delivery.
Brand
Elekta Impac Software
Lot Codes / Batch Numbers
Software Versions (UDI/GTIN): MOSAIQ 2.00 (00858164002305), MOSAIQ 2.20 (00858164002312), MOSAIQ 2.30 (00858164002329), MOSAIQ 2.40 (00858164002077), MOSAIQ 2.41 (00858164002084), MOSAIQ 2.60 -2.64 (00858164002091), MOSAIQ 2.50 (00858164002107), MOSAIQ 2.65 (00858164002220), MOSAIQ 2.70 (00858164002037), MOSAIQ 2.80 (00858164002251), MOSAIQ 2.81 (00858164002282)
Products Sold
Software Versions (UDI/GTIN): MOSAIQ 2.00 (00858164002305); MOSAIQ 2.20 (00858164002312); MOSAIQ 2.30 (00858164002329); MOSAIQ 2.40 (00858164002077); MOSAIQ 2.41 (00858164002084); MOSAIQ 2.60 -2.64 (00858164002091); MOSAIQ 2.50 (00858164002107); MOSAIQ 2.65 (00858164002220); MOSAIQ 2.70 (00858164002037); MOSAIQ 2.80 (00858164002251); MOSAIQ 2.81 (00858164002282)
Elekta Impac Software is recalling MOSAIQ, oncology information system - Product Usage: MOSAIQ is an oncology information system used t due to The user may inadvertently enter Metric values into Height and Weight fields labeled with US Standard Units.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The user may inadvertently enter Metric values into Height and Weight fields labeled with US Standard Units.
Recommended Action
Per FDA guidance
The firm began notifying their consignee on 09/24/2019 by email. The notice explained the issue and provided a workaround for the consignee to use until the updated software is ready for release.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026