FDA Device recall Z-0038-2019
CAPNOSTREAM 20P (INTL) N - ROHS, Part Number CS08652-02
- 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 CS08652-02 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-0038-2019 |
| 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 CS08652-02
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 | B836141168 B836141196 B836141198 B836141206 B836141207 B836141209 B836141210 B836141212 B836141214 B836141217…B836141168 B836141196 B836141198 B836141206 B836141207 B836141209 B836141210 B836141212 B836141214 B836141217 B836141218 B836141221 B836141222 B836141223 B836141225 B836141226 B836141229 B836141230 B837141231 B837141232 B839141793 B840141875 B839141678 B839141682 B839141712 B841142027 B841142029 B841142033 B843142241 B844142389 B844142406 B844142411 B844142423 B844142426 B844142443 B844142449 B847142891 B847142906 B847142923 B847142938 B847142945 B847142947 B848142952 B848142970 B848142994 B848143001 B848143002 B801153800 B803153963 B803153964 B803153965 B803153968 B803153970 B803153971 B803153974 B803153975 B803153979 B803153981 B803153982 B803153983 B803153984 B803153985 B803153990 B841142053 B841142067 B851143673 B852143682 B850143423 B850143424 B850143425 B850143449 B850143450 B852143708 B852143715 B852143719 B852143736 B852143738 B852143743 B852143747 B852143750 B852143751 B852143755 B852143756 B852 |
|---|
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-0038-2019%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.