Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DPM 6 Patient Monitor and DPM 7 Patient Monitor. The Recalled by Mindray DS USA, Inc. dba Mindray North America Due to Mindray has identified an issue that involves the...
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
DPM 6 Patient Monitor and DPM 7 Patient Monitor. The product affected is the Mindray IBP module, P/N is 6800-30-50485 for use with Mindray DPM 6 and DPM 7 patient monitors . Intended to be used for monitoring, displaying, reviewing, storing and alarming of multiple physiological parameters.
Quantity: 455 units
Why Was This Recalled?
Mindray has identified an issue that involves the IBP module used with the DPM 6 and DPM 7 Monitor where the IBP measurement data may be displayed in an incorrect IBP tile on the monitors display.
Where Was This Sold?
This product was distributed to 23 states: AL, CA, CO, FL, GA, IL, IN, IA, LA, MA, MS, MO, MT, NY, NC, ND, OH, PA, SC, TX, VA, WA, WV
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