Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BrightView SPECT gamma camera for Emission Computed Tomography Recalled by Philips Medical Systems (Cleveland) Inc Due to Philips has received one report from the field...
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 SPECT gamma camera for Emission Computed Tomography, Philips Medical Systems, Cleveland, OH 44143 BrightView SPECT is a gamma camera designed for single or dual detector nuclear imaging accommodating a broad range of emission computed tomography Emission Computed Tomography (ECT) studies.
Quantity: 505 units
Why Was This Recalled?
Philips has received one report from the field that there was an unexpected motion of the detector due to a failure of the mechanical assembly.
Where Was This Sold?
This product was distributed to 43 states: AK, AZ, AR, CA, CO, CT, DE, FL, GA, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, SD, TN, TX, VA, WA, WV, WI, WY, 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