Mindray DS USA, Inc.

Frequent Recalls

8

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-10-14 to 2026-10-14

Date	Source	Product	Brand	Severity	Units
2026-10-14	FDA Device	ePM Series Patient Monitor Recall (Oct 2026) – Mindray DS USA	Mindray DS USA, Inc.	Class III	N/A
2026-10-14	FDA Device	BeneVision N1 Recall (Oct 2026) – Mindray DS USA	Mindray DS USA, Inc.	Class III	N/A
2026-10-14	FDA Device	Panorama and Telemetry Monitoring System Recall (Oct 2026)	Mindray DS USA, Inc.	Class III	N/A
2026-10-14	FDA Device	BeneVision Series Telemetry Monitor Recall (Oct 2026)	Mindray DS USA, Inc.	Class III	N/A
2026-10-14	FDA Device	cPM Series Patient Monitor Recall (Oct 2026) – Mindray DS USA	Mindray DS USA, Inc.	Class III	N/A
2026-10-14	FDA Device	T1 Patient Monitor Recall (Oct 2026) – Mindray DS USA	Mindray DS USA, Inc.	Class III	N/A
2026-10-14	FDA Device	BeneView Series Recall (Oct 2026) – Mindray DS USA	Mindray DS USA, Inc.	Class III	N/A
2026-10-14	FDA Device	Passport Series Patient Monitor Recall (Oct 2026)	Mindray DS USA, Inc.	Class III	N/A

Mindray DS USA, Inc. Recalls | WatchRecall