Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DigitalDiagnost Release 3 (Stitching Patient Support) 712025 Recalled by Philips Medical Systems Gmbh, DMC Due to The hook does not securely hold the footplate...
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
DigitalDiagnost Release 3 (Stitching Patient Support) 712025
Why Was This Recalled?
The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
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