Mindray recalls
3 federal recalls on file. We read every CPSC, FDA, USDA and NHTSA notice for Mindray and put it in plain English.
Recent recalls
Mindray patient monitors recalled for unclear alarm manualsMindray is recalling 8 patient and telemetry monitor product lines because some operator's manuals may be insufficient or unclear about certain physiological alarm functions. The FDA classified this as a Class III recall, and no injuries have been reported. About 275,000 units are affected across the included models.
ModerateFDAOct 14, 20268 products
- Check your Mindray BeneVision DMS workstation
Mindray's BeneVision Distributed Monitoring System (DMS) workstations with specific hardware and audio driver configurations may experience audio playback failure or screen freezing during operation. This can affect the usability of the central monitoring system in clinical settings. About 906 units are affected worldwide.
ModerateFDADec 24, 2025
- Mindray V90 vaporizers recalled for anesthesia leakage
Mindray is recalling two models of V90 electronic vaporizers used with its A9 Anesthesia System, sevoflurane and isoflurane. The recall covers a potential for anesthesia leakage. No injuries have been reported, and no remedy has been specified by the FDA.
ModerateFDADec 3, 20252 products