FDA Device recall Z-1003-2026
Philips Incisive CT
- FDA Device
- Class II
- ongoing
- Published 2026-01-14
On 2026-01-14 the FDA classified a Class II recall of Philips Incisive CT by Philips Healthcare Suzhou, citing potential for incomplete scan due to unstable connection inside of floating sensor.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1003-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-12-03 |
| Published | 2026-01-14 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Philips Healthcare Suzhou |
| Distribution | n/a |
Product
Philips Incisive CT
Reason
Potential for incomplete scan due to unstable connection inside of floating sensor.
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1003-2026%22
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