FDA Device recall Z-0742-2013
Mindray DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities
- FDA Device
- Class II
- terminated
- Published 2013-02-06
On 2013-02-06 the FDA classified a Class II recall of Mindray DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities by Mindray Ds Usa D B A Mindray North America, citing mindray has identified an issue with the DPM5 monitors where ST and Arrhythmia features may not be available.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0742-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-09-05 |
| Published | 2013-02-06 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Mindray Ds Usa D B A Mindray North America |
| Distribution | US |
Product
Mindray DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities.
Reason
Mindray has identified an issue with the DPM5 monitors where ST and Arrhythmia features may not be available.
Identifiers
| code_info | p/n 9201F-PA000XX DS- 0C000565 02000335 12000603 12000599 12000597 OCOOO569 9A000247 9A000252 17000648 06000490 05000470 05000466 02000373 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0742-2013%22
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