Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Incisive CT Recalled by Philips North America Due to If the Patient Interface Monitor (PIM) Cable is...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips North America directly.
Affected Products
Incisive CT, Model Numbers 728144 and 728143. Computed Tomography X-Ray System PIM cable part number 459801179871
Quantity: 55 US; 1029 ROW
Why Was This Recalled?
If the Patient Interface Monitor (PIM) Cable is plugged/unplugged frequently as part of daily operation, the connector and wire may disconnect from the welding point, which may result in intermittent loss of the ECG signal. Loss of ECG signal may lead to the decision to rescan the patient or delay in diagnosis during a clinical emergency.
Where Was This Sold?
This product was distributed to 28 states: AL, CA, CO, FL, GA, HI, IL, IN, KS, KY, LA, MD, MI, MS, MO, NE, NJ, NY, ND, OH, OK, PA, RI, SC, TX, UT, VT, WA
About Philips North America
Philips North America has 107 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report