Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is Recalled by Berchtold Corp. Due to During the use of the TELETOM Series 4...
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 Berchtold Corp. directly.
Affected Products
TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is designed for use in operating rooms, medical treatment rooms, intensive care units, or any area of a medical facility that requires a ceiling mounted device to supply power, medical gases, and data-communication services. TELETOM is designed to be used in rooms that have been constructed to meet National Fire Protection Association.
Quantity: 2129 units
Why Was This Recalled?
During the use of the TELETOM Series 4 & 6 there is potential for the controls and brakes not to work properly due to fluid intrusion within the control switches and/or the control board assembly.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Berchtold Corp.
Berchtold Corp. has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report