Mindray DS USA recalls

Mindray DS USA has 47 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 14 Oct 2026. 17 are still ongoing. 11 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls47since 2013

Last 12 months11reported

Class I00% of total

Ongoing17latest 14 Oct 2026

Recalls per month, last 24 months

click a bar for that month

0Dec '24 0 0 0Mar 0 0 0Jun 0 0 0Sep 1 0 3Dec 0 0 0Mar 0 0 0Jun 0 0 0Sep 8 0

Severity split

Class I 0 0%Class II 37 79%Class III 10 21%

Why mindray ds usa is recalled

Product types

By year

2026817%
202549%
202449%
202124%
202036%
201949%
2018715%
201712%
2016511%
201536%

Ongoing mindray ds usa recalls

17 active

Reported	Class	Recall	Company	Reason	Where
14 Oct 2026Device	CLASS III	Passport Series Patient Monitor recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
14 Oct 2026Device	CLASS III	T1 Patient Monitor recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
14 Oct 2026Device	CLASS III	BeneView Series recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
14 Oct 2026Device	CLASS III	cPM Series Patient Monitor recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
14 Oct 2026Device	CLASS III	BeneVision Series Telemetry Monitor recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
14 Oct 2026Device	CLASS III	Panorama and Telemetry Monitoring System recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide

All mindray ds usa recalls, newest first

47 total

Reported	Class	Recall	Company	Reason	Where
14 Oct 2026Device	CLASS III	Passport Series Patient Monitor recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
14 Oct 2026Device	CLASS III	T1 Patient Monitor recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
14 Oct 2026Device	CLASS III	BeneView Series recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
14 Oct 2026Device	CLASS III	cPM Series Patient Monitor recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
14 Oct 2026Device	CLASS III	BeneVision Series Telemetry Monitor recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
14 Oct 2026Device	CLASS III	Panorama and Telemetry Monitoring System recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
14 Oct 2026Device	CLASS III	BeneVision N1 and N-Series Patient Monitor recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
14 Oct 2026Device	CLASS III	ePM Series Patient Monitor recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide
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

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.