FDA Device recall Z-0039-2019
CAPNOSTREAM 20P (INTL) N - ROHS, Part Number CS08652-03
- FDA Device
- Class II
- terminated
- Published 2018-10-10
On 2018-10-10 the FDA classified a Class II recall of CAPNOSTREAM 20P (INTL) N - ROHS, Part Number CS08652-03 by Oridion Medical 1987, citing the date/time, nurse call and alarm settings of the bedside patient monitors may reset to the factory default settings when the monitor is powered off.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0039-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-07-31 |
| Published | 2018-10-10 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Oridion Medical 1987 |
| Distribution | US |
Product
CAPNOSTREAM 20P (INTL) N - ROHS, Part Number CS08652-03
Reason
The date/time, nurse call and alarm settings of the bedside patient monitors may reset to the factory default settings when the monitor is powered off.
Identifiers
| code_info | PA12170508 PA12170656 PA12170657 PA12170702 PA13170746 PA13170769 PA13170777 PA13170782 PA13170783 PA13170786…PA12170508 PA12170656 PA12170657 PA12170702 PA13170746 PA13170769 PA13170777 PA13170782 PA13170783 PA13170786 PA13170787 PA13170798 PA14170801 PA14170802 PA14170803 PA14170807 PA14170808 PA14170811 PA14170812 PA14170813 PA14170814 PA14170815 PA14170816 PA14170817 PA14170818 PA14170819 PA14170820 PA14170821 PA14170822 PA14170823 PA14170824 PA14170825 PA14170826 PA14170827 PA14170828 PA14170829 PA14170830 PA14170831 PA14170832 PA14170833 PA14170834 PA14170835 PA14170836 PA14170837 PA14170838 PA14170839 PA14170840 PA14170841 PA14170842 PA14170843 PA14170844 PA14170845 PA14170846 PA14170847 PA14170848 PA14170849 PA14170850 PA14170851 PA14170852 PA14170853 PA14170854 PA14170855 PA14170856 PA14170857 PA14170858 PA14170859 PA14170860 PA14170861 PA14170862 PA14170863 PA14170864 PA14170865 PA14170866 PA14170867 PA14170868 PA14170869 PA14170870 PA14170871 PA14170872 PA14170873 PA14170874 PA14170875 PA14170876 PA14 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0039-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.