Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BrightView SPECT Recalled by Philips Medical Systems (Cleveland) Inc Due to An issue with the handcontroller may result in...
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, Model Number 882480
Quantity: 696
Why Was This Recalled?
An issue with the handcontroller may result in either spontaneous uncommanded motions or continued motion after the buttons were released.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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