Monaco RTP System Radiation Therapy Treatment Planning System — Class II medical device recall Z-2277-2013
Terminated recall by Elekta, Inc., reported 2013-10-02, distributed in AK, AZ, CA, CO, CT, FL, IL, IN…. Patient needs to be positioned as indicated by the treatment plan.
| Recall number | Z-2277-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Elekta, Inc., Atlanta, GA, United States |
| Recall initiated | 2013-05-22 |
| Classified | 2013-09-25 |
| Reported by FDA | 2013-10-02 |
| Terminated | 2013-12-23 |
| Distributed | 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 |
| Quantity | 72 |
Product
Monaco RTP System Radiation Therapy Treatment Planning System. Radiation treatment planning.
Reason for recall
Patient needs to be positioned as indicated by the treatment plan.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2277-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.