TriFoillmaging Triumph/Triumph II Research CT scanners — Class II medical device recall Z-2833-2016
Terminated recall by Northridge Tri-Modality Imaging,, reported 2016-10-12. The Firm has determined that several Triumph/Triumph II Research CT scanners produced by Northridge Trimodalit
| Recall number | Z-2833-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA mandated |
| Recalling firm | Northridge Tri-Modality Imaging,, Chatsworth, CA, United States |
| Recall initiated | 2016-05-24 |
| Classified | 2016-09-30 |
| Reported by FDA | 2016-10-12 |
| Terminated | 2016-10-06 |
| Quantity | 3 |
Product
TriFoillmaging Triumph/Triumph II Research CT scanners.
Reason for recall
The Firm has determined that several Triumph/Triumph II Research CT scanners produced by Northridge Trimodality Imaging, inc dba TriFoillmaging (or by Gamma Medica-Ideas, Inc and field upgraded with a replacement x-ray tube) may be out of compliance with 21 CFR 1020.40 (Cabinet X-ray standards)
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-2833-2016. 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.