Product Wiki · Recalls · U.S. FDA — Device Enforcement

CAPNOSTREAM 20 (US) N W/PRINTER, Part Number CS08657 — recall Z-0024-2019

U.S. FDA — Device Enforcement · Israel · 2018-07-31 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0024-2019
Date of alert
2018-07-31
Country / jurisdiction
Israel
Risk level
Class II
Risk type
recall
Brand
Oridion Medical 1987 Ltd.
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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