CIC Pro Clinical Information Center Central Station - Product Usage: The intended use is to provide…
Medical device recall Z-0726-2020. Published in FDA’s Enforcement Report on Jan 1, 2020.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Jan 1, 2020. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Not named no state, in where it went
- 41848 units how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
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.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
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.
41848 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Serial Numbers: A0GU1745G A0GU1746G A0GU1747G A0GU1748G A0GU1749G A0GU1750G A0GU1751G A0GU1752G A0GU1756G A0GU1757G A0GU1758G A0GU1759G A0GU1766G A0GU1769G A0GU1770G A0GU1771G A0GU1775G A0GU1788G A0GU1789G A0GU1796G A0GU1799G A0GU1801G…
Every code shown here, 1,996 characters
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 A1GQ0202G A1GQ0203G A1GQ0204G A1GQ0205G A1GQ0206G A1GQ0207G A1GQ0208G A1GQ0209G A1GQ0210G A1GQ0211G A1GQ0212G A1GQ0213G A1GQ0214G A1GQ0216G A1GQ0217G A1GQ0218G A1GQ0219G A1GQ0220G A1GQ0221G A1GQ0222G A1GQ0223G A1GQ0224G A1GQ0225G A1GQ0226G A1GQ0227G A1GQ0228G A1GQ0229G A1GQ0230G A1GQ0231G A1GQ0233G A1GQ0234G A1GQ0235G A1GQ0236G A1GQ0238G A1GQ0239G A1GQ0244G A1GQ0245G A1GQ0246G A1GQ0247G A1GQ0248G A1GQ0249G A1GQ0250G A1GQ0251G A1GQ0252G A1GQ0253G A1GQ0254G A1GU0230G A1GU3167G A1GU3168G A1GU3177G A1GU3178G A1GU3189G A1GU3199G A1GU3200G A23F1180G A23F1181G A23F1182G A23F1185G A23F1186G A23F1187G A23F1188G A23F1189G A23F1190G A23F1191G A23F1195G A23F1196G A23F1197G A23F1198G A23F1199G A23F1202G A23F1206G A23F1208G A23F1209G A23F1210G A23F1211G A23F1212G A23F1213G A23F1214G A23F1215G A23F1218G A23F1219G A23F1220G A23F1223G A23F1224G A23F1225G A23F1226G A23F1227G A23F1228G A23F1229G A23F1230G A23F1231G A23F1232G A23F1233G A23F1234G A23F1235G A23F1236G A23F1237G A23F1239G A23F1240G A23F1246G A23F1247G A23F1248G A23F1249G A23F1250G A23F1251G A23F1252G A23F1253G A23F1257G A23F1258G…
FDA’s list runs to 583,278 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Worldwide distribution.
These words name no state.
The words say it went outside the United States too.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Nov 12, 2019.
- FDA classified it on Dec 20, 2019.
- FDA’s Enforcement Report published it on Jan 1, 2020.
- FDA terminated it on Mar 2, 2026.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- GE Healthcare, LLC, of Waukesha, WI.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 583,278 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
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U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.