Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips DigitalDiagnost software 4.1.x and 4.2.x Recalled by Philips Medical Systems Gmbh, DMC Due to Stitching run on SkyPlate detector interrupted intermittently; Stitching...
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 Gmbh, DMC directly.
Affected Products
Philips DigitalDiagnost software 4.1.x and 4.2.x, A Stationary X-ray System Models: 712027, 712028, 712029, 712031, 712032701032, 712033, 712224, 712225, 712226, 712227, 712228.
Quantity: 829 units
Why Was This Recalled?
Stitching run on SkyPlate detector interrupted intermittently; Stitching with SkyPlate aborts after first image; System software CD contains wrong baseline
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Medical Systems Gmbh, DMC
Philips Medical Systems Gmbh, DMC has 33 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report