Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
OR Table Recalled by Trumpf Medical Systems, Inc. Due to Trumpf has identified six incidents of pinched cables.
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 Trumpf Medical Systems, Inc. directly.
Affected Products
OR Table, Top U26 H V, Model # 1909793; OR Table Top U26 H V U, Model # 1909794; OR Table Top U24 H V, Model # 1909796; OR Table Top U24 H V U, Model # 1909797; OR Table Top U24 H V W, Model # 1909798; OR Table Top U14 H V, Model # 1909799 Product Usage: Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recover from the anesthesia. Patient transport on the operating table top from a patient transfer system to the operating theater or from the operating theater to a patient transfer system.
Quantity: 4 (US) & 229 (Foreign)
Why Was This Recalled?
Trumpf has identified six incidents of pinched cables.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Trumpf Medical Systems, Inc.
Trumpf Medical Systems, Inc. has 30 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report