FDA Device recall Z-0024-2019
CAPNOSTREAM 20 (US) N W/PRINTER, Part Number CS08657
- FDA Device
- Class II
- terminated
- Published 2018-10-10
On 2018-10-10 the FDA classified a Class II recall of CAPNOSTREAM 20 (US) N W/PRINTER, Part Number CS08657 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-0024-2019 |
| 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 (US) N W/PRINTER, Part Number CS08657
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 | B20001115 B20001127 B200001151 B200001164 B200001206 B200001211 B200001254 B200001201 B200001180 B200001220 B…B20001115 B20001127 B200001151 B200001164 B200001206 B200001211 B200001254 B200001201 B200001180 B200001220 B200001236 B200001337 B200001179 B200001246 B200001261 B200001268 B200001293 B200001207 B200001242 B200001215 B200001217 B200001219 B200001247 B200001262 B200001380 B200001213 B200001421 B200001433 B200001442 B200001457 B200001464 B200001523 B200001465 B200001216 B200001455 B200001529 B200001619 B200001621 B200001623 B200001629 B200001649 B200001662 B200001676 B200001504 B200001390 B200001393 B200001575 B200001724 B200001941 B200001988 B200002012 B200002043 B200002084 B200002086 B200002118 B200002193 B400001903 B400002063 B400002083 B400002123 B400002177 B400002212 B400002216 B400002239 B200001804 B200002124 B200002052 B400002241 B400002246 B400002247 B400002254 B400002256 B400002228 B400002245 B400002251 B400002252 B200002127 B200002140 B200002152 B200002155 B200002157 B200001777 B400002026 B40000 |
|---|
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-0024-2019%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.