Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GEMINI TF Big Bore PET/CT Recalled by Philips Medical Systems (Cleveland) Inc Due to The TF Big Bore patient table experienced mechanical...
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 TF Big Bore PET/CT, Computer Tomography System, Philips Healthcare System, Cleveland, OH
Quantity: 47 Units
Why Was This Recalled?
The TF Big Bore patient table experienced mechanical binding during horizontal table motion resulting in an automatic Emergency Stop (E-stop). An E-Stop will interrupt a current scan, resulting in an incomplete study.
Where Was This Sold?
This product was distributed to 21 states: AR, CA, CO, FL, IL, LA, MD, MA, MI, MN, MO, NE, NJ, NY, NC, OH, PA, TX, VT, VA, WI
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