Philips Incisive CT recall (Philips Healthcare (Suzhou) Co., Ltd.)
Medical deviceClass IIOngoing
Summary: Philips Healthcare (Suzhou) Co., Ltd. is recalling Philips Incisive CT. Reason: Potential for incomplete scan due to unstable connection inside of floating sensor.
What is being recalled
Philips Incisive CT
Why
Potential for incomplete scan due to unstable connection inside of floating sensor.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
U.S. and U.S. territories
How to tell if yours is affected
No lot or model codes were published. Match the product description above.
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-1003-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | December 3, 2025 |
| Reported | January 14, 2026 |
| Company | Philips Healthcare (Suzhou) Co., Ltd. |
| Company location | Suzhou, China |
| Initiated by | FDA Mandated |
| Quantity | 35 |
More recalls from Philips Healthcare (Suzhou) Co., Ltd. · all medical device recalls · recalls from December 2025