Brilliance Big Bore Radiology CT with 4 — Class II medical device recall Z-0839-2018
Terminated recall by Philips Medical Systems (Cleveland) Inc, reported 2018-03-14, distributed nationwide. Software issues including: Software errors that may result in Extended Field of View check message not display
| Recall number | Z-0839-2018 |
|---|---|
| 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 | 2018-01-03 |
| Classified | 2018-03-02 |
| Reported by FDA | 2018-03-14 |
| Terminated | 2019-07-02 |
| Distributed | Nationwide (US) |
| Quantity | 119 |
| Reason classes | software |
| Serial numbers | 760001, 760002, 760003, 760004, 760005, 760006, 760007, 760008, 760009, 76001, 760010, 760011, 760012, 760013, 760014, 760015, 760016, 760017, 760018, 760019, 760020, 760021, 760022, 760023, 760024 and 94 more |
| Model numbers | 728244 |
Product
Brilliance Big Bore Radiology CT with 4.2.0 software version. Model #' 728244 Product Usage: 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. These devices may include signal analysts and display equipment, patient and equipment supports, components, and accessories.
Reason for recall
Software issues including: Software errors that may result in Extended Field of View check message not displayed when Field of View is set >600 mm for a paused scan; Request for change to automatically turn on the center x/y 0 setting and the disable result rotation setting when turning on the CT simulation Exam Card; Software errors that may result in Tumor LOC allowing POI (Point of Interest) locking when a non-isocenter slice is displayed; Software errors that may result in partial set of images or inability to generate CT images.
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-0839-2018. 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.