Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Healthcare TraumaDiagnost Recalled by Philips Electronics North America Corporation Due to If arm is not fastened securely it could...
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 Electronics North America Corporation directly.
Affected Products
Philips Healthcare TraumaDiagnost; Codes: 72001, 720011, 720013, 720020; A radiological examination unit for emergency work and routine skeletal diagnosis.
Quantity: 399 distributed, 262 are subject to this event
Why Was This Recalled?
If arm is not fastened securely it could fall down.
Where Was This Sold?
This product was distributed to 10 states: AL, CA, FL, GA, KS, MA, NY, RI, TX, WI
About Philips Electronics North America Corporation
Philips Electronics North America Corporation has 160 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report