FDA · Medical devices ·
Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144. recall
Philips Healthcare (Suzhou) Co., Ltd. recalled Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144. on September 2, 2026 because of potential of failing to trigger clinical scan during Bolus Tracking. It was sold nationwide.
Why it was recalled
Potential of failing to trigger clinical scan during Bolus Tracking.
What's recalled
Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144.
Quantity: N/A
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Philips Healthcare (Suzhou) Co., Ltd., Suzhou, N/A
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
U.S. Nationwide and U.S. Territories distribution. - Status
- Ongoing
- Recall number
- Z-2988-2026
- Source
- U.S. Food and Drug Administration
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