FDA Device recall Z-0020-2019
CAPNOSTREAM 20 (US) N, Part Number CS08651
- FDA Device
- Class II
- terminated
- Published 2018-10-10
On 2018-10-10 the FDA classified a Class II recall of CAPNOSTREAM 20 (US) N, Part Number CS08651 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-0020-2019 |
| 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 20 (US) N, Part Number CS08651
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 | B200001468 B200001473 B200001476 B200001594 B200001951 B200001980 B200001992 B200002054 B200002129 B200002144…B200001468 B200001473 B200001476 B200001594 B200001951 B200001980 B200001992 B200002054 B200002129 B200002144 B200002147 B200002149 B200002164 B200002171 B200002204 B200002154 B200001956 B200002085 B200002110 B200001948 B200002048 B200002167 B200002168 B200001953 B200001955 B200001961 B200001964 B200001966 B200001968 B200001969 B200001972 B200001981 B200001991 B200002001 B200002006 B200002008 B200002022 B200002024 B200002033 B200002034 B200002074 B200002075 B200002080 B200002095 B200002111 B200002126 B200001985 B200001717 B200001422 B200001505 B200001599 B200001691 B200001696 B200001783 B200001889 B200001916 B200001919 B200001923 B200002115 B400002214 B400002220 B400002222 B400002223 B200001373 B200001430 B200001480 B200001492 B200001499 B200001534 B200001707 B200001711 B200001720 B200001767 B200001769 B200001868 B200001882 B200001885 B200001887 B200001924 B200001928 B200001935 B200001936 B200001937 B200 |
|---|
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-0020-2019%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.