ONCOR Avant Garde — Class II medical device recall Z-0168-2016
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2015-11-04, distributed nationwide. potential safety risk of collision of the LINAC gantry with the patient or the treatment table in case of auto
| Recall number | Z-0168-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc, Malvern, PA, United States |
| Recall initiated | 2015-05-05 |
| Classified | 2015-10-27 |
| Reported by FDA | 2015-11-04 |
| Terminated | 2017-05-05 |
| Distributed | Nationwide (US) |
| Quantity | 158 |
| Serial numbers | 2855, 2894, 2958, 3068, 3103, 3114, 3133, 3136, 3186, 3203, 3225, 3241, 3244, 3245, 3274, 3285, 3296, 3302, 3303, 3305, 3318, 3361, 3367, 3383, 3413 and 132 more |
Product
ONCOR Avant Garde, ONCOR Impression Plus, ONCOR Expression, ONCOR Impression, PRIMUS HI, MEVATRON M2/PRIMUS Mid-Energy, ARTISTE; intended use is to deliver x-ray radiation for therapeutic treatment of cancer.
Reason for recall
potential safety risk of collision of the LINAC gantry with the patient or the treatment table in case of automatically sequenced treatment delivery techniques using SIMTEC" Auto Field Sequence Option.
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-0168-2016. 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.