Philips Incisive Ct
Philips Incisive CT Recall Summary Philips is recalling the Incisive CT scanner because an internal connection in the floating sensor may become unstable, which could result in incomplete CT scans. This is a Class II recall affecting the Incisive CT product line. The affected devices are manufactured by Philips Healthcare (Suzhou) Co., Ltd.
- Recalling firm
- Philips Healthcare (Suzhou) Co., Ltd. Suzhou Industrial Park No.
- Product
- Philips Incisive CT
- Reason
- Potential for incomplete scan due to unstable connection inside of floating sensor.
- Classification
- Class II
- Category
- consumer product recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2025-12-03
- Status
- Open, Classified
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/5d9eb057-4fc9-4ba8-9bc9-69a66391ef4d