Mindray DPM5 Monitor — Class II medical device recall Z-0742-2013
Terminated recall by Mindray DS USA, Inc. d.b.a. Mindray North America, reported 2013-02-06, distributed nationwide. Mindray has identified an issue with the DPM5 monitors where ST and Arrhythmia features may not be available.
| Recall number | Z-0742-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mindray DS USA, Inc. d.b.a. Mindray North America, Mahwah, NJ, United States |
| Recall initiated | 2012-09-05 |
| Classified | 2013-01-27 |
| Reported by FDA | 2013-02-06 |
| Terminated | 2013-10-22 |
| Distributed | Nationwide (US) |
| Quantity | 13 units |
Product
Mindray DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities.
Reason for recall
Mindray has identified an issue with the DPM5 monitors where ST and Arrhythmia features may not be available.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0742-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.