FDA Device recall Z-1082-2014
Desktop Pro TM linear accelerator control software intended to assist a licensed practitioner in the delivery of radiation to defined targe…
- FDA Device
- Class II
- terminated
- Published 2014-03-12
On 2014-03-12 the FDA classified a Class II recall of Desktop Pro TM linear accelerator control software intended to assist a licensed practitioner in the delivery of radiation to defined targe… by Elekta, citing during the treatment table, gantry, and collimator calibration procedures, it is possible to type incorrect values or invert a value.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1082-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-11-25 |
| Published | 2014-03-12 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Elekta |
| Distribution | US |
Product
Desktop Pro TM linear accelerator control software intended to assist a licensed practitioner in the delivery of radiation to defined target volumes.
Reason
During the treatment table, gantry, and collimator calibration procedures, it is possible to type incorrect values or invert a value.
Identifiers
| code_info | Identifier - 6.0, 6.1.0, 7.0.1 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1082-2014%22
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