PlainRecalls
FDA Devices Moderate Class II Ongoing

Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil, Model Number: 728325.

Reported: October 1, 2025 Initiated: August 13, 2025 #Z-2603-2025

Product Description

Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil, Model Number: 728325.

Reason for Recall

The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.

Details

Recalling Firm
Philips North America Llc
Units Affected
3 units
Distribution
Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Czech Republic, Denmark, Egypt, France, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Latvia, Lebanon, Mauritius, Mexico, Netherlands, Norway, Peru, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, T¿rkiye, United Kingdom, Utd.Arab.Emir., Vietnam.
Location
Cambridge, MA

Frequently Asked Questions

What product was recalled?
Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil, Model Number: 728325.. Recalled by Philips North America Llc. Units affected: 3 units.
Why was this product recalled?
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 1, 2025. Severity: Moderate. Recall number: Z-2603-2025.