FDA Device recall Z-0023-2019
CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-03
- 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 CS08651-03 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-0023-2019 |
| 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 CS08651-03
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 | PA07170091 PA07170092 PA07170093 PA07170094 PA07170095 PA07170096 PA07170097 PA07170098 PA07170099 PA07170100…PA07170091 PA07170092 PA07170093 PA07170094 PA07170095 PA07170096 PA07170097 PA07170098 PA07170099 PA07170100 PA07170101 PA07170102 PA07170103 PA07170104 PA07170106 PA07170107 PA07170108 PA07170109 PA07170110 PA07170111 PA07170112 PA07170113 PA07170114 PA07170115 PA07170116 PA07170117 PA07170118 PA07170119 PA09170121 PA09170123 PA09170124 PA09170126 PA09170127 PA09170128 PA09170129 PA09170130 PA09170131 PA09170132 PA09170133 PA09170134 PA09170135 PA09170136 PA09170137 PA09170138 PA09170139 PA09170140 PA09170141 PA09170142 PA09170143 PA09170144 PA09170145 PA09170146 PA09170147 PA09170148 PA09170149 PA09170150 PA09170151 PA09170152 PA09170153 PA09170154 PA09170155 PA09170156 PA09170157 PA09170158 PA09170159 PA09170160 PA10170161 PA10170162 PA10170163 PA10170164 PA10170165 PA10170166 PA10170167 PA10170168 PA10170169 PA10170170 PA10170172 PA10170173 PA10170174 PA10170175 PA10170176 PA10170177 PA10170178 PA10 |
|---|
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-0023-2019%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.