FDA Device recall Z-1724-2014
Synergy XVI Intended for radiation therapy treatment
- FDA Device
- Class II
- terminated
- Published 2014-06-25
On 2014-06-25 the FDA classified a Class II recall of Synergy XVI Intended for radiation therapy treatment by Elekta, citing XVI can incorrectly calculate the target position of the treatment table.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1724-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-04-23 |
| Published | 2014-06-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Elekta |
| Distribution | AZ, CT, IA, MD, MI, MN, NV, OH, TX, VA |
Product
Synergy XVI Intended for radiation therapy treatment.
Reason
XVI can incorrectly calculate the target position of the treatment table.
Identifiers
| code_info | XVI R4.0 to R4.2.1, R4.5.0, R4.5.1, and R5.0.0 to R5.0.1 |
|---|
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-1724-2014%22
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