Every recall we track for Mindray DS USA, Inc. dba Mindray North America — 24 in all — plus the complaints and injury reports the public filed about them.
Mindray recalls BeneVision Distributed Monitoring hardware with audio driver version 6.0.9484.1 due to possible audio playback failure or screen freezing. Affected units include specific HP Pro Mini 400 G9 models.
Mindray recalls Isoflurane V90 Electronic Vaporizers with A9 Anesthesia System due to potential anesthesia leakage. Affected units have specific serial numbers and part numbers.
Mindray recalls Sevoflurane V90 Electronic Vaporizers with A9 Anesthesia System due to potential anesthesia leakage. Affected units have specific serial numbers and part numbers.
Mindray recalls BeneVision N1 Patient Monitors with specific part numbers and software versions due to potential for abnormal alarm pause. Affected units may require correction to prevent monitoring errors.
Mindray recalls Sevoflurane E_Vap Quik-Fil used with A9 Anesthesia System due to potential overdose risk from inaccurate anesthetic delivery. Patients may experience drowsiness or neurological issues if anesthetic concentration is too high.
Mindray recalls Isoflurane E_Vap Safety Filling Adapters used with A9 Anesthesia Systems due to potential over-delivery of anesthetic. Patients may experience drowsiness or neurological issues if overdose occurs.
Mindray recalls Desflurane E_Vap (Saf-T-Fill) used with A9 Anesthesia System due to potential over-delivery of anesthetic. Patients may experience drowsiness or neurological issues if overdose occurs.
Mindray recalls Sevoflurane E_Vap Safety Filling Adapters for A9 Anesthesia Systems due to potential high anesthetic output causing patient drowsiness or neurological issues. Affected units have specific serial numbers.
Mindray recalls 3AA battery cradles for BeneVision TD60 and TM80 Telepacks that may not power on properly. Affected units include specific model numbers and part numbers.
Mindray BeneVision Distributed Monitoring System (DMS) with specific software versions may freeze, causing patients to lose monitoring data. Affected units include models 115-051209-00 and 115-034414-00/115-034413-00 with software versions 03.04.00 through 04.04.01.
Mindray recalls DP-30 ultrasound systems with 65EC10EA transducers that may display incorrect needle-guide brackets. This could affect imaging accuracy during medical exams.
Mindray recalls BA-800M Chemistry Analyzers with specific part numbers due to potential gas spring failure causing low risk of arm, hand or finger injury.
Mindray recalls ABS800 Chemistry Analyzers with specific part numbers due to potential gas spring failure causing low risk of injury to arms, hands, or fingers.
Mindray recalls Accutorr 7 monitors with software version 8.1.5 due to unapproved enhancements in NIBP valve assembly board that may cause inaccurate blood pressure readings.
Mindray recalls Rosie4 Vital Signs Monitors with software version 8.1.5 due to potential NIBP hose blockage. Affected units have specific part numbers and were sold in professional healthcare settings.
Mindray recalls Rosebud Vital Signs Monitors with software version 8.1.5 due to unapproved enhancements in the NIBP valve assembly board that may affect monitoring accuracy.
Mindray recalls Accutorr 3 Vital Signs Monitors with specific software version 8.1.5 that may have NIBP valve assembly problems. Affected units could have unapproved software features that might cause hose blockages.
Mindray recalls BeneVision DMS software versions 03.01.00 to 03.03.00 due to ECG waveforms showing flat lines when more than 64 TD60 transmitters are connected to a central station.
Mindray recalls Hematology Diluent M-53D (20L) used with BC-5390 analyzers due to potential elevated platelet counts. Affected lots include 2017060105, 2017041106, 2017010701, 2016121401, 2016112301, 2016111302.
Mindray recalls specific lots of M-30D hematology diluent for BC-3200/3600 analyzers that may cause elevated platelet counts in blood tests.
Mindray recalls Gas Module 3 spirometers (part 115-030108-00) purchased between Feb 2008 and Oct 2015 due to regulatory changes requiring new safety approvals. This update ensures continued safe use in medical settings.
