Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
OmniDiagnost Classic X-ray system Angiographic and Diagnostic Recalled by Philips Medical Systems Nederlands Due to The fixation of the upper and lower tilt...
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 Nederlands directly.
Affected Products
OmniDiagnost Classic X-ray system Angiographic and Diagnostic, Product Nos. 70859, 708023, 708024, 708025
Quantity: 477
Why Was This Recalled?
The fixation of the upper and lower tilt actuator, of the Omnidiagnost system might break off and the table will start to rotate from 0 to + 90 /- 90 degree with high speed. This rotating movement can not be stopped by the user. This could potentially lead to the patient falling off the table. There is a risk of injury for the patient, user, or bystander.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Medical Systems Nederlands
Philips Medical Systems Nederlands has 79 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report