Philips recalled 6 CT 6000 systems on August 13, 2025. The patient support table may descend unexpectedly due to a ball screw misalignment. This recall affects devices distributed worldwide, including the U.S.
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Philips North America Llc or your healthcare provider for instructions. Notification method: Letter
The recall includes Philips CT 6000, Model Number: 728307. The affected serial numbers are 87150, 87169, 87118, 87168, 87166, and 87164. These units were distributed worldwide.
The patient support table may descend unexpectedly to its lowest position. This poses a high risk of injury to patients during examination.
No injuries have been reported to date. The recall has been classified as high hazard due to the potential for serious injury.
Stop using the CT system immediately. Follow the recall instructions provided by Philips North America. Contact your healthcare provider for further instructions.
For more information, contact Philips North America at 1-800-XXX-XXXX. Visit the FDA's recall page for additional resources.
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