Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1 Recalled by Philips North America Llc Due to Potential table stop due to a broken tabletop...
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 ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1 (Model 706110)- A multi-functional general radiography and fluoroscopy (R/F) system
Quantity: Total Quantity: 234 units. US 195units. R.O.W 39 units
Why Was This Recalled?
Potential table stop due to a broken tabletop cable: On the ProxiDiagnost N90 table there is a cable located under the tabletop that is covered by a plastic sleeve which can crack and damage the cable. If the tabletop cable breaks, the user may not be able to initiate table tilting movements or braking
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips North America Llc
Philips North America Llc has 301 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report