Brilliance iCT & Brilliance iCT SP Computed Tomography X-Ray Systems — Class II medical device recall Z-0832-2014
Terminated recall by Philips Medical Systems (Cleveland) Inc, reported 2014-02-05, distributed nationwide. Patient images exhibited ring artifacts.
| Recall number | Z-0832-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Medical Systems (Cleveland) Inc, Cleveland, OH, United States |
| Recall initiated | 2013-12-09 |
| Classified | 2014-01-27 |
| Reported by FDA | 2014-02-05 |
| Terminated | 2014-05-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, IL |
| Quantity | 7 units |
| Serial numbers | 100018, 100040, 100411, 100503, 100506, 200047, 200121 |
Product
Brilliance iCT & Brilliance iCT SP Computed Tomography X-Ray Systems, Philips Healthcare, Cleveland, OH The Brilliance iCT and iCT SP are whole body Computed Tomography X-Ray Systems intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. This device may include signal analysis and display equipment, patient and equipment supports, components and accessories.
Reason for recall
Patient images exhibited ring artifacts.
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-0832-2014. 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.