FDA Device recall Z-0026-2019
CAPNOSTREAM 20P (US) N W/PRINTER, Part Number CS08657-01
- 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 W/PRINTER, Part Number CS08657-01 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-0026-2019 |
| 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 W/PRINTER, Part Number CS08657-01
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 | B400002777 B400002778 B400002779 B400002780 B400002781 B400002782 B400002783 B400002784 B400002785 B400002786…B400002777 B400002778 B400002779 B400002780 B400002781 B400002782 B400002783 B400002784 B400002785 B400002786 B600002902 B600002903 B600002905 B600002906 B600002908 B600002901 B600002904 B600002907 B632123517 B633123526 B621135542 B621135543 B621135544 B621135545 B621135546 B621135547 B621135548 B621135549 B621135550 B621135551 B621135552 B621135553 B621135554 B621135555 B621135556 B621135557 B621135558 B621135559 B621135560 B621135561 B621135562 B621135564 B621135566 B621135568 B621135569 B621135570 B621135571 B621135572 B621135573 B621135574 B621135575 B621135577 B621135578 B621135580 B621135582 B621135583 B621135584 B621135585 B621135586 B621135587 B621135589 B621135590 B621135591 B621135592 B621135594 B621135595 B621135588 B621135593 B633137055 B633137058 B633137060 B633137061 B633137062 B633137063 B633137064 B633137065 B633137066 B633137068 B633137069 B634137070 B634137071 B634137072 B634137073 B634 |
|---|
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-0026-2019%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.