Mindray DS USA, Inc. dba Mindray North America recalls
Every recall we track for Mindray DS USA, Inc. dba Mindray North America — 24 in all, from 2017–2025 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Mindray DS USA, Inc. dba Mindray North America peaked in 2019 (6); 24 since 2017. 4% rated “stop using now”.
All FDA recall records for Mindray DS USA, Inc. dba Mindray North America since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 1 | 3 | 0 | 4 |
| 2018 | 0 | 0 | 3 | 0 | 3 |
| 2019 | 0 | 0 | 6 | 0 | 6 |
| 2020 | 0 | 0 | 1 | 0 | 1 |
| 2021 | 0 | 0 | 2 | 0 | 2 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 1 | 3 | 0 | 0 | 4 |
| 2025 | 0 | 3 | 1 | 0 | 4 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Mindray DS USA, Inc. dba Mindray North America recalls
What to do if you have a recalled Mindray DS USA, Inc. dba Mindray North America product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Mindray DS USA, Inc. dba Mindray North America recalls
14 shown- Use cautionMedical device
Mindray DS USA, Inc. dba Mindray North America recalls Hardware configuration of the BeneVision Central Monitoring System (CMS), marketed as BeneVision Distributed Monitoring
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.
MindrayNov 18, 2025 - Use cautionMedical device
Mindray DS USA, Inc. dba Mindray North America recalls Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following: 1. Sev E_Vap.
Mindray recalls Sevoflurane V90 Electronic Vaporizers with A9 Anesthesia System due to potential anesthesia leakage. Affected units have specific serial numbers and part numbers.
MindrayOct 20, 2025 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017, 6660E-PA00014, 6660E-PA00012, 6660E-PA00011,
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.
MindrayAug 15, 2025 - Stop using nowMedical device
Mindray DS USA, Inc. dba Mindray North America recalls Sevoflurane E_Vap.(Safety Filling adapter) used with the A9 Anesthesia System-Used to provide the vapor of an
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.
MindrayJul 22, 2024 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls 3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60 Telepack (Model Number 115-047566-00
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.
MindrayMay 27, 2021 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00 2. p/n 115-034414-00 and 115-034413-00 when
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.
MindrayFeb 22, 2021 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls DP-30 Digital Ultrasonic Diagnostic Imaging System, Part No. 1155E-PA00004 - Product Usage: The Digital Ultrasonic
Mindray recalls DP-30 ultrasound systems with 65EC10EA transducers that may display incorrect needle-guide brackets. This could affect imaging accuracy during medical exams.
MindrayJan 13, 2020 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls ABS800 Chemistry Analyzer Part Number BA81F-PA00001, Containing Gas spring YQ-8/18-90-272-180N (Material Code
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.
MindrayDec 9, 2019 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls Accutorr 3 Vital Signs Monitor with NIBP valve assembly board, p/n 115-017679-00, containing software version 8.1.5 -
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.
MindrayOct 1, 2019 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls Mindray BeneVision Distributed Monitoring System (DMS), Part No. 115-034413-00
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.
MindrayAug 30, 2018 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls Hematology Diluent M-30D used with BC-3200 and BC-3600 Hematology Analyzer; Part Numbers: (1) 105-005405-00 (2 x 5.5L
Mindray recalls specific lots of M-30D hematology diluent for BC-3200/3600 analyzers that may cause elevated platelet counts in blood tests.
MindrayJan 24, 2018 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls Gas Module 3 monitoring spirometer, Part Number: 115-030108-00 Product Usage: The Gas Module 3 is an accessory device
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.
MindrayDec 1, 2017 - Use cautionMedical device
Mindray DS USA, Inc. dba Mindray North America recalls TD60 Transmitter battery charger used with the BeneVision Central Station, Part number 115-030108-00
Mindray recalls TD60 Transmitter battery chargers (part 115-030108-00) due to risk of battery swelling and separation. Affected units may need replacement.
MindrayJul 14, 2017 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls A-Series A7 Anesthesia Delivery System; Model Number: 0632F-PA0000X (A7) Product Usage: The A-Series Anesthesia System
Mindray recalls A7 Anesthesia Delivery System model 0632F-PA0000X (2013-2016) due to software error potentially skipping startup leak test. Affected units may apply wrong settings during anesthesia delivery.
MindrayJul 14, 2017
Mindray DS USA, Inc. dba Mindray North America recall questions
How many recalls has Mindray DS USA, Inc. dba Mindray North America had?
24 recalls from Mindray DS USA, Inc. dba Mindray North America are on record with U.S. safety agencies, from 2017–2025.
What is the most recent Mindray DS USA, Inc. dba Mindray North America recall?
Mindray DS USA, Inc. dba Mindray North America recalls Hardware configuration of the BeneVision Central Monitoring System (CMS), marketed as BeneVision Distributed Monitoring, dated Nov 18, 2025. Every Mindray DS USA, Inc. dba Mindray North America recall is listed on this page, newest first.
Why are Mindray DS USA, Inc. dba Mindray North America products recalled?
The most common reasons on record: Potential for anesthesia leakage. (2).
What should I do if I have a recalled Mindray DS USA, Inc. dba Mindray North America product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Mindray DS USA, Inc. dba Mindray North America recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.