Mindray DS USA, Inc. dba Mindray North America: Medical Device Recalls in 2021

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Mindray DS USA, Inc. dba Mindray North America in 2021. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00 2. p/n 115-034414-00 and 115-034413-00 when used with the following software versions: 03.04.00 04.01.00 04.03.00 04.04.00 04.04.01
3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60 Telepack (Model Number 115-047566-00 /115-060044-00) and TM80 Telepack (Model Number 115-047565-00 / 120-018867-00). Used with physiological data monitor.