Philips Healthcare (Suzhou) Co., Ltd. is recalling 35 Philips Incisive CT systems due to a defect in the floating sensor's internal connection. This unstable connection can cause the scanner to stop working unexpectedly during a medical procedure, resulting in an incomplete scan. If this happens, a patient may need to undergo a repeat scan, which leads to unnecessary additional radiation exposure and potential delays in diagnosis or treatment.
An unstable connection inside the floating sensor can cause the imaging system to fail mid-scan. This creates a risk of diagnostic errors or requires repeat medical procedures, exposing patients to more radiation than intended.
Correction or replacement of the unstable connection in the floating sensor.
Recall Number: Z-1003-2026; Affects 35 units total.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
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Sources: FDA iRES · Raw API Response
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