Mindray DPM 7 Monitor — Class II medical device recall Z-2737-2015
Terminated recall by Mindray DS USA, Inc. dba Mindray North America, reported 2015-09-16, distributed in CT, IA, KY, MS, PA, UT, WA. The DPM 7 Monitors may display a black screen.
| Recall number | Z-2737-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mindray DS USA, Inc. dba Mindray North America, Mahwah, NJ, United States |
| Recall initiated | 2015-07-27 |
| Classified | 2015-09-04 |
| Reported by FDA | 2015-09-16 |
| Terminated | 2017-05-02 |
| Distributed | CT, IA, KY, MS, PA, UT, WA |
| Quantity | 13 units |
| Lot numbers | 14A18, 6800F-PA00001 |
| Serial numbers | 46002583, DU-46002587, DU-46002588, DU-46002589, DU-46002592, DU-46002594, DU-46002595, DU-46002596, DU-46002599, DU-46002600, DU-46002601, DU-46002605, DU-46002606 |
Product
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.
Reason for recall
The DPM 7 Monitors may display a black screen.
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-2737-2015. 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.