Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DigitalDiagnost C90 High Performance. radiography and fluoroscopy system Recalled by Philips Medical Systems DMC GmbH Due to Following a system restart where the Table Height...
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 C90 High Performance. radiography and fluoroscopy system
Quantity: 140 systems in total, (Updated 1/30/2023).
Why Was This Recalled?
Following a system restart where the Table Height 2 (TH2) is the default setting and then switched to Wallstand VS2, operators will see an incorrect orientation of image on the first examination due to an issue in the firmware of the Wallstand VS2 board. The system will rotate the amplimat field selection by 90 degrees. The wrong amplimat field selection may cause an incorrect dose of radiation to occur. Additionally, the anatomic position markers may become mispositioned and could potentially be associated with the opposite side of the anatomy. (Updated 1/30/23) Expansion of the root cause to include incorrect amplimat field selection by 90 degrees following the first exposure using Wallstand VS2 and a subsequent system restart. Previously, this issue only occurred following a system restart where the Table Height 2 (TH2) is the default setting.
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