Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Mindray DPM 7 Monitor Recalled by Mindray DS USA, Inc. dba Mindray North America Due to The DPM 7 Monitors may display a black...
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. dba Mindray North America directly.
Affected Products
Mindray DPM 7 Monitor, Multi Parameter Patient Monitor (with Arrhythmia Detection and Alarms) Intended to be used for monitoring, displaying, reviewing, storing and alarming of multiple physiological parameters including ECG (3-lead or 5-lead selectable), arrhythmia detection, ST Segment analysis, and heart rate.
Quantity: 13 units
Why Was This Recalled?
The DPM 7 Monitors may display a black screen.
Where Was This Sold?
This product was distributed to 7 states: CT, IA, KY, MS, PA, UT, WA
About Mindray DS USA, Inc. dba Mindray North America
Mindray DS USA, Inc. dba Mindray North America has 39 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report