FDA Device recall Z-0025-2019
CAPNOSTREAM 20P (US) N W/PRINTER - ROHS, Part Number CS08657-02
- FDA Device
- Class II
- terminated
- Published 2018-10-10
On 2018-10-10 the FDA classified a Class II recall of CAPNOSTREAM 20P (US) N W/PRINTER - ROHS, Part Number CS08657-02 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-0025-2019 |
| 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 (US) N W/PRINTER - ROHS, Part Number CS08657-02
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 | B819140007 B819140026 B819140032 B819140038 B819140050 B819140051 B819140052 B819140054 B819140060 B819140063…B819140007 B819140026 B819140032 B819140038 B819140050 B819140051 B819140052 B819140054 B819140060 B819140063 B820140069 B839141801 B839141803 B840141814 B840141819 B840141820 B840141823 B840141826 B839141802 B839141805 B839141807 B839141808 B839141809 B839141811 B839141812 B839141813 B840141815 B840141816 B840141818 B840141821 B840141822 B840141824 B840141827 B840141828 B840141829 B840141830 B840141831 B840141832 B840141833 B840141834 B840141835 B840141837 B840141838 B840141839 B840141843 B840141844 B840141847 B840141848 B840141849 B840141850 B819140004 B819140006 B819140008 B819140011 B819140012 B819140017 B819140020 B819140021 B819140031 B819140033 B819140037 B819140043 B819140045 B819140048 B819140034 B841142048 B844142441 B844142455 B845142604 B847142950 B848143034 B848143039 B848143043 B848143053 B848143084 B848143096 B848143104 B849143117 B849143118 B849143120 B849143121 B849143122 B849143123 B849 |
|---|
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-0025-2019%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.