Mindray North America recalls
4 recalls filed under Mindray North America. The most recent was published December 24, 2025.
-
Class II · 10 months ago
Mindray North America Hardware configuration of the BeneVision Central Monitoring recall: When the Worstation of the BeneVision DMS has a specific hardware
When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen…
-
Class II · 11 months ago
Mindray North America Isoflurane V90 Electronic Vaporizer with the A9 Anesthesia recall: Potential for anesthesia leakage
Potential for anesthesia leakage.
-
Class II · 11 months ago
Mindray North America Sevoflurane V90 Electronic Vaporizer with the A9 Anesthesia recall: Potential for anesthesia leakage
Potential for anesthesia leakage.
-
Class II · 1+ years ago
Mindray North America BeneVision N1 Patient Monitor . Part Numbers: 6660E-PA00017 recall: Potential for activation of an abnormal alarm pause
Potential for activation of an abnormal alarm pause.
About this page
Mindray North America appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.