Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical Systems, Inc. Due to Complaints received of the front joint of the...
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
Trumpf Ceiling Mounted Surgical Lighting Systems,Helion/Xenion S/M/L, User Manual #1441784. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
Quantity: 9,287 units total
Why Was This Recalled?
Complaints received of the front joint of the spring arm AC 2000 could break at the interface to the monitor.
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