Class II — Mindray DS USA, Inc. d.b.a. Mindray North America
| Recalling firm | Mindray DS USA, Inc. |
|---|---|
| Registered facility | MINDRAY DS USA, Inc. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Mindray has identified an issue with the DPM5 monitors where ST and Arrhythmia features may not be available. |
| Product | Mindray DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities. |
| Quantity | 13 units |
| Distribution | US Nationwide Distribution including the states of: VA, TN, FL, & TX |
| Initiated | 2012-09-05 |
| Classified | 2013-01-27 |
| Terminated | 2013-10-22 |
| Recall number | Z-0742-2013 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Mindray DS USA, Inc. d.b.a. Mindray North America (Z-0742-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/63800/
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