FDA Device recall Z-2277-2013
Monaco RTP System Radiation Therapy Treatment Planning System
- 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 Therapy Treatment Planning System by Elekta, citing patient needs to be positioned as indicated by the treatment plan.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2277-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-05-22 |
| Published | 2013-10-02 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Elekta |
| Distribution | AK, AZ, CA, CO, CT, FL, IL, IN, MA, MD, MI, MN, MO, NC, NJ, NM, NY, OH, OK, OR, PA, PR, RI, SC, TN, TX, VA, WA |
Product
Monaco RTP System Radiation Therapy Treatment Planning System. Radiation treatment planning.
Reason
Patient needs to be positioned as indicated by the treatment plan.
Identifiers
| code_info | All versions of Monaco |
|---|
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-2277-2013%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.