Mindray DS USA recalls

Mindray DS USA has 39 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 24 Dec 2025. 9 are still ongoing. 3 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls39since 2013

Last 12 months3reported

Class I00% of total

Ongoing9latest 24 Dec 2025

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 1 0Nov 3 0 0Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 37 95%Class III 2 5%

Why mindray ds usa is recalled

Product types

By year

2025410%
2024410%
202125%
202038%
2019410%
2018718%
201713%
2016513%
201538%
2014513%

Ongoing mindray ds usa recalls

9 active

Reported	Class	Recall	Company	Reason	Where
24 Dec 2025Device	CLASS II	Hardware configuration of the BeneVision Central Monitoring recalled	Mindray DS USA	Device Malfunction	Nationwide
3 Dec 2025Device	CLASS II	The Anesthesia System is a device used to administer recalled	Mindray DS USA	Packaging Defects	Nationwide
3 Dec 2025Device	CLASS II	The Anesthesia System is a device used to administer recalled	Mindray DS USA	Packaging Defects	Nationwide
1 Oct 2025Device	CLASS II	BeneVision N1 Patient Monitor (N1) recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
11 Sep 2024Device	CLASS II	Sevoflurane E_Vap.(Quik-Fil):used recalled by Mindray DS USA	Mindray DS USA	Packaging Defects	8 states
11 Sep 2024Device	CLASS II	Isoflurane E_Vap.(Safety Filling adapter): used recalled	Mindray DS USA	Packaging Defects	8 states

All mindray ds usa recalls, newest first

39 total

Reported	Class	Recall	Company	Reason	Where
24 Dec 2025Device	CLASS II	Hardware configuration of the BeneVision Central Monitoring recalled	Mindray DS USA	Device Malfunction	Nationwide
3 Dec 2025Device	CLASS II	The Anesthesia System is a device used to administer recalled	Mindray DS USA	Packaging Defects	Nationwide
3 Dec 2025Device	CLASS II	The Anesthesia System is a device used to administer recalled	Mindray DS USA	Packaging Defects	Nationwide
1 Oct 2025Device	CLASS II	BeneVision N1 Patient Monitor (N1) recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
11 Sep 2024Device	CLASS II	Sevoflurane E_Vap.(Quik-Fil):used recalled by Mindray DS USA	Mindray DS USA	Packaging Defects	8 states
11 Sep 2024Device	CLASS II	Isoflurane E_Vap.(Safety Filling adapter): used recalled	Mindray DS USA	Packaging Defects	8 states
11 Sep 2024Device	CLASS II	Desflurane E_Vap.(Saf-T-Fill) used recalled by Mindray DS USA	Mindray DS USA	Packaging Defects	8 states
11 Sep 2024Device	CLASS II	Sevoflurane E_Vap.(Safety Filling adapter) used recalled	Mindray DS USA	Packaging Defects	8 states
28 Jul 2021Device	CLASS III	3AA battery cradle recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
24 Mar 2021Device	CLASS II	Mindray BeneVision Distributed Monitoring System( DMS) recalled	Mindray DS USA	Device Malfunction	Nationwide
26 Feb 2020Device	CLASS II	DP-30 Digital Ultrasonic Diagnostic Imaging System recalled	Mindray DS USA	Other	Nationwide
5 Feb 2020Device	CLASS II	BA-800M Chemistry Analyzer Part Numbers BA81E-PA00002 recalled	Mindray DS USA	Device Malfunction	MI, TX
5 Feb 2020Device	CLASS II	ABS800 Chemistry Analyzer recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	MI, TX
6 Nov 2019Device	CLASS II	Accutorr 7 Vital Signs Monitor with NIBP valve assembly board recalled	Mindray DS USA	Temperature Abuse	Nationwide
6 Nov 2019Device	CLASS II	Rosie4 Vital Signs Monitor with NIBP valve assembly board recalled	Mindray DS USA	Temperature Abuse	Nationwide
6 Nov 2019Device	CLASS II	Rosebud Vital Signs Monitor with NIBP valve assembly board recalled	Mindray DS USA	Temperature Abuse	Nationwide
6 Nov 2019Device	CLASS II	Accutorr 3 Vital Signs Monitor with NIBP valve assembly board recalled	Mindray DS USA	Temperature Abuse	Nationwide
24 Oct 2018Device	CLASS II	Mindray BeneVision Distributed Monitoring System (DMS) recalled	Mindray DS USA	Other	9 states
18 Apr 2018Device	CLASS II	Hematology Diluent M-53D used with BC-5390 Hematology Analyzer recalled	Mindray DS USA	Other	6 states
18 Apr 2018Device	CLASS II	Hematology Diluent used with and Hematology Analyzer recalled	Mindray DS USA	Other	6 states
4 Apr 2018Device	CLASS III	Gas Module 3 monitoring spirometer recalled by Mindray DS USA	Mindray DS USA	Other	Nationwide
14 Mar 2018Device	CLASS II	A-Series A3/A5 Anesthesia Delivery System recalled by Mindray DS USA	Mindray DS USA	Packaging Defects	Nationwide
14 Mar 2018Device	CLASS II	A-Series A7 Anesthesia Delivery System recalled by Mindray DS USA	Mindray DS USA	Packaging Defects	Nationwide
14 Feb 2018Device	CLASS II	TD60 Transmitter battery charger used recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	27 states
5 Jul 2017Device	CLASS II	TI Transport Monitor/Module Battery Pack recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
9 Nov 2016Device	CLASS II	TD60 display Telemetry Transmitter recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	NJ
7 Sep 2016Device	CLASS II	A7 Anesthesia Delivery System recalled by Mindray DS USA	Mindray DS USA	Packaging Defects	Nationwide
24 Aug 2016Device	CLASS II	Passport Series Patient Monitor intended for monitoring recalled	Mindray DS USA	Packaging Defects	Nationwide
4 May 2016Device	CLASS II	Panorama Patient Monitoring Network Mindray DS USA recalled	Mindray DS USA	Device Malfunction	Nationwide
10 Feb 2016Device	CLASS II	Panorama Patient Monitoring Network recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.