FDA Device recall Z-0236-2015
Philips Brilliance iCT Computed Tomography X-Ray System Product Usage: The Brilliance iCT/Brilliance iCT SP is a Computed Tomography X-Ray…
- FDA Device
- Class II
- terminated
- Published 2014-12-24
On 2014-12-24 the FDA classified a Class II recall of Philips Brilliance iCT Computed Tomography X-Ray System Product Usage: The Brilliance iCT/Brilliance iCT SP is a Computed Tomography X-Ray… by Philips Medical Systems, citing it was discovered that a software defect may result in the scanner not terminating the CT scan at the intended location.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0236-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-07-31 |
| Published | 2014-12-24 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Philips Medical Systems |
| Distribution | n/a |
Product
Philips Brilliance iCT Computed Tomography X-Ray System Product Usage: The Brilliance iCT/Brilliance iCT SP is a Computed Tomography X-Ray System intended to produce crosssectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. (d) A description of the defect in the
Reason
It was discovered that a software defect may result in the scanner not terminating the CT scan at the intended location.
Identifiers
| code_info | Software version 4.1. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0236-2015%22
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