TD60 display Telemetry Transmitter — Class II medical device recall Z-0321-2017
Terminated recall by Mindray DS USA, Inc. dba Mindray North America, reported 2016-11-09. Mindray has become aware that the TD60 Display Telemetry Transmitter used with the BeneVision Central Station
| Recall number | Z-0321-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mindray DS USA, Inc. dba Mindray North America, Mahwah, NJ, United States |
| Recall initiated | 2016-09-08 |
| Classified | 2016-10-28 |
| Reported by FDA | 2016-11-09 |
| Terminated | 2017-05-04 |
| Countries outside the US | CA |
| Quantity | 1,278 units |
| Reason classes | packaging |
| Serial numbers | HHA59001430, HHA59001439, HHA59001450 |
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 for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0321-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.