Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0321-2017 — 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

U.S. FDA — Device Enforcement · United States · 2016-09-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0321-2017
Date of alert
2016-09-08
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Mindray DS USA, Inc. dba Mindray North America
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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