Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Mindray DPM5 Monitor Recalled by Mindray DS USA, Inc. d.b.a. Mindray North America Due to Mindray has identified an issue with the DPM5...

Date: September 5, 2012
Company: Mindray DS USA, Inc. d.b.a. Mindray North America
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Mindray DS USA, Inc. d.b.a. Mindray North America directly.

Affected Products

Mindray DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities.

Quantity: 13 units

Why Was This Recalled?

Mindray has identified an issue with the DPM5 monitors where ST and Arrhythmia features may not be available.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Mindray DS USA, Inc. d.b.a. Mindray North America

Mindray DS USA, Inc. d.b.a. Mindray North America has 9 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report