DPM 6 Patient Monitor and DPM 7 Patient Monitor — Class II medical device recall Z-0837-2015
Terminated recall by Mindray DS USA, Inc. dba Mindray North America, reported 2014-12-31, distributed in AL, CA, CO, FL, GA, IA, IL, IN…. Mindray has identified an issue that involves the IBP module used with the DPM 6 and DPM 7 Monitor where the I
| Recall number | Z-0837-2015 |
|---|---|
| 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 | 2014-10-06 |
| Classified | 2014-12-19 |
| Reported by FDA | 2014-12-31 |
| Terminated | 2017-06-06 |
| Distributed | AL, CA, CO, FL, GA, IA, IL, IN, LA, MA, MO, MS, MT, NC, ND, NY, OH, PA, SC, TX, VA, WA, WV |
| Quantity | 455 units |
Product
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.
Reason for recall
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.
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-0837-2015. 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.