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. 4 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls39since 2013

Last 12 months4reported

Class I00% of total

Ongoing9latest 24 Dec 2025

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 1Oct 0 3 0Jan '26 0 0 0Apr 0 0 0Jul 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 to recalled	Mindray DS USA	Packaging Defects	Nationwide
3 Dec 2025Device	CLASS II	The Anesthesia System is a device used to administer to 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	Nationwide
11 Sep 2024Device	CLASS II	Isoflurane E_Vap.(Safety Filling adapter): used recalled	Mindray DS USA	Packaging Defects	Nationwide

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 to recalled	Mindray DS USA	Packaging Defects	Nationwide
3 Dec 2025Device	CLASS II	The Anesthesia System is a device used to administer to 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	Nationwide
11 Sep 2024Device	CLASS II	Isoflurane E_Vap.(Safety Filling adapter): used recalled	Mindray DS USA	Packaging Defects	Nationwide
11 Sep 2024Device	CLASS II	Desflurane E_Vap.(Saf-T-Fill) used recalled by Mindray DS USA	Mindray DS USA	Packaging Defects	Nationwide
11 Sep 2024Device	CLASS II	Sevoflurane E_Vap.(Safety Filling adapter) used recalled	Mindray DS USA	Packaging Defects	Nationwide
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

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.