Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips TraumaDiagnost- a Stationary X-Ray System (Bucky System) Model: 720013 Recalled by Philips North America, LLC Due to If the shaft breaks due to material fatigue,...
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, LLC directly.
Affected Products
Philips TraumaDiagnost- a Stationary X-Ray System (Bucky System) Model: 720013 - Product Usage: general radiography.
Quantity: 346 units (5 US and 341 OUS)
Why Was This Recalled?
If the shaft breaks due to material fatigue, the trauma arm can fall down and may result in injury.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips North America, LLC
Philips North America, LLC has 88 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report