FDA Device recall Z-0022-2019
CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-02
- 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 - ROHS, Part Number CS08651-02 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-0022-2019 |
| 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 - ROHS, Part Number CS08651-02
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 | B836141101 B836141102 B836141103 B836141104 B836141106 B836141107 B836141108 B836141109 B836141110 B836141111…B836141101 B836141102 B836141103 B836141104 B836141106 B836141107 B836141108 B836141109 B836141110 B836141111 B836141113 B836141116 B836141117 B836141118 B836141119 B836141120 B836141121 B836141122 B836141123 B836141124 B836141125 B836141126 B836141127 B836141128 B836141130 B836141131 B836141133 B836141134 B836141135 B836141136 B836141137 B836141138 B836141139 B836141140 B836141141 B836141142 B836141143 B836141144 B836141145 B836141146 B836141147 B836141148 B836141149 B836141150 B836141151 B836141152 B836141153 B836141154 B836141155 B836141156 B836141157 B836141158 B836141159 B836141160 B836141161 B836141162 B836141163 B836141164 B836141165 B836141166 B836141167 B836141169 B836141170 B836141172 B836141173 B836141174 B836141175 B836141176 B836141177 B836141105 B836141112 B836141179 B836141180 B836141181 B836141182 B836141184 B836141185 B836141186 B836141187 B836141188 B836141189 B836141190 B836141192 B836 |
|---|
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-0022-2019%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.