Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GEMINI PET/CT System Recalled by Philips Medical Systems (Cleveland) Inc Due to The reason for this inspection is to determine...
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 Medical Systems (Cleveland) Inc directly.
Affected Products
GEMINI PET/CT System, a diagnostic imaging system for fixed or mobile installations that combines Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems.
Quantity: 264 units
Why Was This Recalled?
The reason for this inspection is to determine if the Spindle Block Servo Controllers on the CT subsystem of potentially affected GEMINI PET/CT systems are susceptible to premature failure.
Where Was This Sold?
This product was distributed to 35 states: AL, AZ, CA, CO, DE, FL, GA, HI, IL, IN, KS, KY, LA, MD, MA, MO, NE, NV, NJ, NM, NY, ND, OH, OK, OR, PA, RI, TN, TX, UT, VA, WA, WV, WI, WY
About Philips Medical Systems (Cleveland) Inc
Philips Medical Systems (Cleveland) Inc has 313 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report