FDA Device recall Z-0726-2020
CIC Pro Clinical Information Center Central Station - Product Usage: The intended use is to provide clinicians with adult, pediatric and ne…
- FDA Device
- Class II
- terminated
- Published 2020-01-01
On 2020-01-01 the FDA classified a Class II recall of CIC Pro Clinical Information Center Central Station - Product Usage: The intended use is to provide clinicians with adult, pediatric and ne… by Ge Healthcare, citing when connected to the Mission Critical (MC) and /or Information Exchange (IX) networks, certain versions of the CARESCAPE Telemetry Server, ApexPro Telemetry Server, CARESCAPE Cen….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0726-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-11-12 |
| Published | 2020-01-01 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Ge Healthcare |
| Distribution | n/a |
Product
CIC Pro Clinical Information Center Central Station - Product Usage: The intended use is to provide clinicians with adult, pediatric and neonatal patient data in a centralized location within a hospital or clinical environment. CIC Pro Clinical Information Center central station is intended to collect information from a network and display this data. This data includes physiological, patient demographic and/or other nonmedical information.
Reason
When connected to the Mission Critical (MC) and /or Information Exchange (IX) networks, certain versions of the CARESCAPE Telemetry Server, ApexPro Telemetry Server, CARESCAPE Central Station (CSCS) version 1 and Central Information Center (CIC) systems were identified to have vulnerabilities to a cyber-attack.
Identifiers
| code_info | Serial Numbers: A0GU1745G A0GU1746G A0GU1747G A0GU1748G A0GU1749G A0GU1750G A0GU1751G A0GU1752G A0GU1756G A0G…Serial Numbers: A0GU1745G A0GU1746G A0GU1747G A0GU1748G A0GU1749G A0GU1750G A0GU1751G A0GU1752G A0GU1756G A0GU1757G A0GU1758G A0GU1759G A0GU1766G A0GU1769G A0GU1770G A0GU1771G A0GU1775G A0GU1788G A0GU1789G A0GU1796G A0GU1799G A0GU1801G A0GU1802G A0GU1805G A0GU1806G A0GU1807G A0GU1808G A0GU1809G A0GU1810G A0GU1813G A0GU1814G A0GU1816G A0GU1823G A0GU1824G A0GU1825G A0GU1826G A0GU1827G A0GU1829G A0GU1830G A0GU1831G A0GU1832G A0GU1833G A0GU1834G A0GU1835G A0GU1839G A0GU1840G A0GU1841G A0GU1842G A0GU1845G A0GU1846G A0GU1847G A0GU1848G A0GU1849G A0GU1850G A0GU1851G A0GU1852G A0GU1853G A0GU1854G A0GU1855G A0GU1856G A0GU1857G A0GU1858G A0GU1859G A0GU1860G A0GU1865G A0GU1866G A0GU1867G A0GU1868G A0GU1869G A0GU1870G A0GU1871G A0GU1872G A0GU1873G A0GU1874G A0GU1875G A0GU1876G A0GU1877G A0GU1878G A0GU1881G A0GU1882G A0GU1885G A0GU1887G A0GU1888G A0GU1894G A0GU1895G A1GQ0198G A1GQ0199G A1GQ0200G A1GQ0201G A1GQ |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0726-2020%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.