Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BrightView XCT Recalled by Philips North America Due to While using Pre-Programmed Motion during an extrinsic quality...
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 North America directly.
Affected Products
BrightView XCT, Gamma Camera, Product Code 882482
Quantity: 135 US; 294 OUS
Why Was This Recalled?
While using Pre-Programmed Motion during an extrinsic quality assurance scan, a gap is created between the patient support and the detector, which may present a potential extremity entrapment hazard. Risk to patients may include fracture, body part loss of function/debilitation, muscle or ligament sprain or strain, laceration, crush injury, abrasion, or contusion.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips North America
Philips North America has 107 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report