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Berchtold Corp. recalls TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is designed for use in operating rooms, medical treatment ro
Recalled October 28, 2015 · FDA recall Z-0154-2016 · Berchtold
Hazard
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. · FDA Class II
Units
2129 units
Sold at
Worldwide Distribution - US (nationwide), Canada, and Germany
Description
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.
Product
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.
Manufacturer(s)
Berchtold Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →