FDA Device recall Z-0036-2019
CAPNOSTREAM 20 (INTL) N, Part Number CS08652
- FDA Device
- Class II
- terminated
- Published 2018-10-10
On 2018-10-10 the FDA classified a Class II recall of CAPNOSTREAM 20 (INTL) N, Part Number CS08652 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-0036-2019 |
| 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 (INTL) N, Part Number CS08652
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 | B200001301 B200001306 B200001625 B200002065 B200002206 B200001982 B200002098 B200001475 B200002000 B200001865…B200001301 B200001306 B200001625 B200002065 B200002206 B200001982 B200002098 B200001475 B200002000 B200001865 B200001835 B200001944 B200002030 B200002202 B200001012 B200001314 B200001866 B200002032 B200002139 B200001723 B200001908 B200001926 B200001703 B200001755 B200001500 B200001763 B200001519 B200001653 B200001655 B200001661 B200001670 B200001722 B400001155 B400002342 B200001729 B400002520 B400002480 B400002505 B200001802 B400002492 B400002518 B400002521 B400002542 B400002728 B400002713 B400002800 B400002813 B451113083 B450113072 B406123152 B406123163 B408123213 B400002450 B410123265 B420123420 B420123421 B400002844 B440112971 B447123778 B449123886 B449123889 B449123899 B449123915 B449123917 B449123919 B449123920 B449123921 B449123922 B449123924 B449123925 B449123927 B449123930 B449123931 B449123936 B449123938 B449123939 B449123963 B449123967 B450123979 B450123982 B450123983 B450123985 B450123989 B450 |
|---|
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-0036-2019%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.