Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DigitalDiagnost 4 (1) High Performance Recalled by Philips Medical Systems DMC GmbH Due to Philips has identified that some ceiling suspension telescopic...
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 DMC GmbH directly.
Affected Products
DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 712032;
Quantity: 12 units
Why Was This Recalled?
Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Medical Systems DMC GmbH
Philips Medical Systems DMC GmbH has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report