Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BrightView XCT: product code 882482 Recalled by Philips Medical Systems (Cleveland) Inc Due to Flat Panel Display (FPD) failed to remain securely...
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
BrightView XCT: product code 882482, BrightView X- upgraded with the XCT Flat Panel Detector (FPD): product code 882454. Gamma camera for Single Photon Emission Computed Tomography (SPECT) Medical Device for imaging.
Quantity: 407
Why Was This Recalled?
Flat Panel Display (FPD) failed to remain securely locked in the deployed position.
Where Was This Sold?
This product was distributed to 32 states: AZ, CA, CO, FL, GA, HI, IL, IA, KY, MD, MA, MN, MS, MO, MT, NE, NV, NJ, NY, NC, ND, OH, OK, OR, PA, SD, TX, VT, WA, WV, WI, DC
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