FDA Device recall Z-0321-2017

TD60 display Telemetry Transmitter, SHENZHEN Mindray Bio-Medical Electronics Co., LTD, Mindray Building, Keji 12th Road South, Hi-Tech Indu…

FDA Device
Class II
terminated
Published 2016-11-09

On 2016-11-09 the FDA classified a Class II recall of TD60 display Telemetry Transmitter, SHENZHEN Mindray Bio-Medical Electronics Co., LTD, Mindray Building, Keji 12th Road South, Hi-Tech Indu… by Mindray Ds Usa, citing mindray has become aware that the TD60 Display Telemetry Transmitter used with the BeneVision Central Station may crack on the bezel surrounding the display and also the transmitt….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0321-2017
Classification	Class II
Status	terminated
Initiated	2016-09-08
Published	2016-11-09
Last updated	2026-09-13 11:54 UTC
Company	Mindray Ds Usa
Distribution	n/a

Product

TD60 display Telemetry Transmitter, SHENZHEN Mindray Bio-Medical Electronics Co., LTD, Mindray Building, Keji 12th Road South, Hi-Tech Industrial Partk, Nanshan, Shenzhen, 518057 P.R. China

Reason

Mindray has become aware that the TD60 Display Telemetry Transmitter used with the BeneVision Central Station may crack on the bezel surrounding the display and also the transmitter may not power on or will power on but display an error message.

Identifiers

code_info	p/n 115-029485-00, Serial #'s HHA59001430, HHA59001439, HHA59001450 thru HHA59001460, HHA59001537, HHA59001540, HHA5900… p/n 115-029485-00, Serial #'s HHA59001430, HHA59001439, HHA59001450 thru HHA59001460, HHA59001537, HHA59001540, HHA59001549 thru HHA59001550, HHA59001591,HHA59001609, HHA59001615, HHA59001626, HHA59001632, HHA5A003110, HHA5A003113 thru HHA5A003115, HHA5A003118 thru HHA5A003119, HHA5C004233, HHA5C004485, HHA59001420 thru HHA59001429, HHA5B003441 thru HHA5B003450, HHA5C004059, HHA5C004065, HHA5C004075, HHA5C004077, HHA5C004091, HHA5C004095 thru HHA5C004097, HHA5C004102, HHA5C004106, HHA57000155 thru HHA57000161, HHA57000163 thru HHA57000168, HHA57000171, HHA57000173 thru HHA57000180, HHA57000182 thru HHA57000184, HHA57000195 thru HHA57000199, HHA57000201 thru HHA57000205, HHA57000207, HHA57000209 thru HHA57000223, HHA58001037, HHA59001386, HHA59001432, HHA5A003075, HHA5A003079, HHA5A003264, HHA5B003365, HHA5B003386, HHA5B003451 thru HHA5B003452, HHA5B003877, HHA5B003880, HHA5C004098, HHA5C004104, HHA5C004110, HHA5C004113, HHA5C004126, HHA5C004134, HHA5C004200, HHA5C004464, HHA5C004470, H

code_info

p/n 115-029485-00, Serial #'s HHA59001430, HHA59001439, HHA59001450 thru HHA59001460, HHA59001537, HHA59001540, HHA5900…

p/n 115-029485-00, Serial #'s HHA59001430, HHA59001439, HHA59001450 thru HHA59001460, HHA59001537, HHA59001540, HHA59001549 thru HHA59001550, HHA59001591,HHA59001609, HHA59001615, HHA59001626, HHA59001632, HHA5A003110, HHA5A003113 thru HHA5A003115, HHA5A003118 thru HHA5A003119, HHA5C004233, HHA5C004485, HHA59001420 thru HHA59001429, HHA5B003441 thru HHA5B003450, HHA5C004059, HHA5C004065, HHA5C004075, HHA5C004077, HHA5C004091, HHA5C004095 thru HHA5C004097, HHA5C004102, HHA5C004106, HHA57000155 thru HHA57000161, HHA57000163 thru HHA57000168, HHA57000171, HHA57000173 thru HHA57000180, HHA57000182 thru HHA57000184, HHA57000195 thru HHA57000199, HHA57000201 thru HHA57000205, HHA57000207, HHA57000209 thru HHA57000223, HHA58001037, HHA59001386, HHA59001432, HHA5A003075, HHA5A003079, HHA5A003264, HHA5B003365, HHA5B003386, HHA5B003451 thru HHA5B003452, HHA5B003877, HHA5B003880, HHA5C004098, HHA5C004104, HHA5C004110, HHA5C004113, HHA5C004126, HHA5C004134, HHA5C004200, HHA5C004464, HHA5C004470, H

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0321-2017%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.