Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is… — Class II medical device recall Z-0987-2017
Terminated recall by Elekta, Inc., reported 2017-01-18, distributed nationwide. Cross profile for Varian 60 degree wedge shows "horns."
| Recall number | Z-0987-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Elekta, Inc., Atlanta, GA, United States |
| Recall initiated | 2016-12-23 |
| Classified | 2017-01-09 |
| Reported by FDA | 2017-01-18 |
| Terminated | 2021-07-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, AT, AU, BB, BG, BR, CA, CH, CN, CW, CZ, DE, DK, ES, FI, FR, GB, GR, HN, HU, ID, IE, IN, IS, IT, JP, KE, KR, MY, NL, NO, OM, PE, PL, PT, RO, RU, SE, SK, TH, TR, TW, ZA |
| Quantity | 433 |
Product
Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation therapy planning software designed to analyze and plan radiation treatment is three dimensions for the purpose of treating patients with cancer.
Reason for recall
Cross profile for Varian 60 degree wedge shows "horns."
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-0987-2017. 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.