FDA Medical Device Recalls (openFDA)
Mindray DS USA, Inc. dba Mindray North America: Mindray BeneVision Distributed Monitoring System (DMS), Part No. 115-034413-00
- Recall number
- Z-0170-2019
- Recalling firm
- Mindray DS USA, Inc. dba Mindray North America
- Product
- Mindray BeneVision Distributed Monitoring System (DMS), Part No. 115-034413-00
- Status
- Terminated
- Initiated
- 2018-08-30
- Posted
- not on file
- Terminated
- 2018-12-20
- Reason
- The firm has identified performance anomalies with the device caused when more than 64 TD60 telemetry transmitters have been connected to a central station. The anomaly causes some ECG waveforms to appear as a flat line at the centralized viewing station and will manifest if more than 64 TD60 transmitters have been connected to a given central station server. Each central station supports only 32 transmitters at a time. For the issue to manifest, the BeneVision DMS needs to be configured to use flexible device assignment, have more than 64 TD60 transmitters, and the workflow must allow 64 TD60s to move around between multiple central stations in the same care area.
- Root cause
- Software design
- Action
- The firm notified affected consignees on August 30, 2018, via Urgent Medical Device Recall letter. The letter advised customers of the software issue when more than 64 telemetry transmitters have been connected to a central station. Customers were advised to use the system normally, but informed that a Mindray Service Representative would be in contact to arrange for a system software update to be performed at the customer site. Mindrays Technical Support team may be reached at (877) 913-9663 (Option 1), Monday through Friday, 8:30am - 5:30pm ET should you have technical questions. Customers were also asked to complete and return an attached Acknowledgement and Receipt Form.
- Quantity
- 5
- Distribution
- Distributed to accounts in CA, CO, FL, MA, NY, PA, PR, TX, and WV.
- Lot, serial or model codes
- This potential issue affects BeneVision DMS with software version 03.01.00 to 03.03.00
- 510(k) numbers
- K162607
- PMA numbers
- not on file
- Product code
- MHX
- Firm FEI
- 2221819
- Firm city
- Mahwah
- Firm state
- NJ
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28