FDA Device recall Z-0154-2016

TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is designed for use in operating rooms, medical treatment rooms, intensive care…

FDA Device
Class II
terminated
Published 2015-10-28

On 2015-10-28 the FDA classified a Class II recall of TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is designed for use in operating rooms, medical treatment rooms, intensive care… by Berchtold, citing 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 contro….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0154-2016
Classification	Class II
Status	terminated
Initiated	2015-09-23
Published	2015-10-28
Last updated	2026-09-13 11:53 UTC
Company	Berchtold
Distribution	US

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.

Reason

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.

Identifiers

code_info	Serial # W62920, W62920, W62919, U61431, V61880, V61879, V61878, V61877, V61865, V61864, V61863, V61862, V61… Serial # W62920, W62920, W62919, U61431, V61880, V61879, V61878, V61877, V61865, V61864, V61863, V61862, V61861, V61860, V61859, V61858, V61857, V61856, V62216, V62636, U61281, U61116, U61114, U61113, W62973, W62972, V62440, V62439, V62438, V62437, V62429, V62428, V62427, V62426, V62425, V62424, V62420, V62419, V62412, V62411, T60420, T60499, T60498, T60497, T60496, T60493, T60492, T60491, T60490, T60489, T60488, V62454, V62453, V62452, V62160, V62159, V61808, V61807, U61488, U61480, U61479, U61432, U61358, U61357, U61357, U61356, U61355, U61352, U61351, U61350, U61349, U61338, U61337, U61336, U61335, U61334, U61333, U61332, U61331, U61330, U61329, U61328, U61314, U61313, U61312, U61244, U61242, U61241, U61240, U60273, V61965, V62367, V62306, V61966, V61813, V61812, V61811, V61810, T60099, T60098, T60097, T60096, T60096, T60095, T60092, T60080, T60079, T60075, T60072, T60071, T6

code_info

Serial # W62920, W62920, W62919, U61431, V61880, V61879, V61878, V61877, V61865, V61864, V61863, V61862, V61…

Serial # W62920, W62920, W62919, U61431, V61880, V61879, V61878, V61877, V61865, V61864, V61863, V61862, V61861, V61860, V61859, V61858, V61857, V61856, V62216, V62636, U61281, U61116, U61114, U61113, W62973, W62972, V62440, V62439, V62438, V62437, V62429, V62428, V62427, V62426, V62425, V62424, V62420, V62419, V62412, V62411, T60420, T60499, T60498, T60497, T60496, T60493, T60492, T60491, T60490, T60489, T60488, V62454, V62453, V62452, V62160, V62159, V61808, V61807, U61488, U61480, U61479, U61432, U61358, U61357, U61357, U61356, U61355, U61352, U61351, U61350, U61349, U61338, U61337, U61336, U61335, U61334, U61333, U61332, U61331, U61330, U61329, U61328, U61314, U61313, U61312, U61244, U61242, U61241, U61240, U60273, V61965, V62367, V62306, V61966, V61813, V61812, V61811, V61810, T60099, T60098, T60097, T60096, T60096, T60095, T60092, T60080, T60079, T60075, T60072, T60071, T6

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0154-2016%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.