FDA Device recall Z-0037-2019
CAPNOSTREAM 20P (INTL) N, Part Number CS08652-01
- 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, Part Number CS08652-01 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-0037-2019 |
| 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, Part Number CS08652-01
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 | B642138114 B642138116 B642138122 B643138126 B643138128 B643138132 B643138134 B643138139 B643138144 B643138146…B642138114 B642138116 B642138122 B643138126 B643138128 B643138132 B643138134 B643138139 B643138144 B643138146 B643138150 B643138153 B643138156 B643138160 B643138166 B643138167 B643138168 B643138169 B643138170 B643138171 B643138172 B643138175 B643138177 B643138179 B643138181 B643138182 B643138190 B643138192 B643138215 B643138216 B643138217 B643138218 B643138219 B643138222 B643138224 B643138225 B643138228 B643138230 B643138232 B643138233 B643138240 B643138241 B643138243 B643138245 B643138253 B644138256 B644138259 B644138286 B644138287 B644138291 B610148829 B610148834 B610148838 B610148845 B611148924 B611148945 B611148946 B611148951 B612149038 B612149039 B615149045 B615149050 B615149054 B615149060 B615149062 B615149063 B615149070 B615149071 B615149073 B615149074 B615149086 B615149088 B615149090 B621149514 B622149593 B622149651 B622149654 B622149655 B622149658 B622149660 B622149663 B622149664 B622149665 B622 |
|---|
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-0037-2019%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.