Recall database

Mindray DS USA, Inc. dba Mindray North America recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–4 of 4 recalls

Class IIOngoingZ-0920-2026

Mindray DS USA, Inc. Dba Mindray North America recalls Hardware configuration of the BeneVision Central Monitoring System (CMS)

When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen freezing.

Mindray DS USA, Inc. d…NJDec 24, 2025

Class IIOngoingZ-0721-2026

Mindray DS USA, Inc. Dba Mindray North America recalls Isoflurane (ISO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the…

Potential for anesthesia leakage.

Mindray DS USA, Inc. d…NJDec 3, 2025

Class IIOngoingZ-0720-2026

Mindray DS USA, Inc. Dba Mindray North America recalls Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as t…

Potential for anesthesia leakage.

Mindray DS USA, Inc. d…NJDec 3, 2025

Class IIOngoingZ-2622-2025

Mindray DS USA, Inc. Dba Mindray North America recalls BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017

Potential for activation of an abnormal alarm pause.

Mindray DS USA, Inc. d…NJOct 1, 2025