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.
Other recalls by Mindray Ds Usa D B A Mindray North America
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FDA Device · Class II · 2013-04-03 · Mindray Ds Usa D B A Mindray North America - Mindray DS USA, Inc., DPM Central Monitoring System with ambulatory Telepack
FDA Device · Class II · 2013-02-20 · Mindray Ds Usa D B A Mindray North America - DPM Central Station Mindray DS USA, Inc. 800 MacArthur Boulevard, Mahwah, NJ 07430 The Central Monitoring Station (CMS) network transfers i…
FDA Device · Class II · 2013-01-09 · Mindray Ds Usa D B A Mindray North America - Mindray V12 Size: 320 mm X 320 mm X 450 mm N.W.: 3 kg G.W.: 6 kg Qty:1 Manufactured in China Mindray V21 Size: 515 mm X 335 mm X 685 mm N.W…
FDA Device · Class II · 2012-12-26 · Mindray Ds Usa D B A Mindray North America - DPM 6/7 Patient Monitor Manufactured in China for : Mindray DS USA, Inc. 800 MacArthur Blvd
FDA Device · Class II · 2012-12-19 · Mindray Ds Usa D B A Mindray North America
All Mindray Ds Usa D B A Mindray North America recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0742-2013%22
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