Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Berchtold Chromophare F528 Surgical Lights. Product Usage: The medical lights Recalled by Stryker Communications Due to The back cover of the light head was...
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 Stryker Communications directly.
Affected Products
Berchtold Chromophare F528 Surgical Lights. Product Usage: The medical lights are for usage in hospital treatment rooms. They provide localized lighting focused on the patient s body for detecting and treating disease, injury, and disability. The surgical lights may only be used in rooms used for medical purposes that have been equipped in accordance with VDE 0100-710 or IEC 60364-7-10 in accordance with the regulations.
Quantity: 946 lights
Why Was This Recalled?
The back cover of the light head was insufficiently assembled and could potentially fall off the light.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Communications
Stryker Communications has 18 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report