Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to The firm became aware of an issue where...
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 X, model #882478; gamma camera designed for single or dual detector nuclear imaging
Quantity: 117 units
Why Was This Recalled?
The firm became aware of an issue where during a non-Auto Body Contouring (ABC), non-circular, rel-180 scan, the detector may come in contact with the patient. The issue was caused by a software defect in the workflow setup script.
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