Philips Incisive CT — Class II medical device recall Z-1003-2026
Ongoing recall by Philips Healthcare (Suzhou) Co., Ltd., reported 2026-01-14. Potential for incomplete scan due to unstable connection inside of floating sensor.
| Recall number | Z-1003-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | FDA mandated |
| Recalling firm | Philips Healthcare (Suzhou) Co., Ltd., Suzhou, China |
| Recall initiated | 2025-12-03 |
| Classified | 2026-01-08 |
| Reported by FDA | 2026-01-14 |
| Quantity | 35 |
Product
Philips Incisive CT
Reason for recall
Potential for incomplete scan due to unstable connection inside of floating sensor.
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-1003-2026. 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.