FDA Device recall Z-2276-2013
Monaco RTP System Radiation treatment planning
- FDA Device
- Class II
- terminated
- Published 2013-10-02
On 2013-10-02 the FDA classified a Class II recall of Monaco RTP System Radiation treatment planning by Elekta, citing upgrade installation script is designed to overwrite the same pouch files in the Treatment Couch Library with the original default values.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2276-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-07-02 |
| Published | 2013-10-02 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Elekta |
| Distribution | US |
Product
Monaco RTP System Radiation treatment planning
Reason
Upgrade installation script is designed to overwrite the same pouch files in the Treatment Couch Library with the original default values.
Identifiers
| code_info | Versions 3.10.00 and later |
|---|
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-2276-2013%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.