Reported Feb 26, 2014 · Terminated

GE Healthcare, Dash 3000, Dash 4000 and Dash 5000 Patient Monitors, Dash Port2 Docking Station.

GE Healthcare, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: GE Healthcare, LLC · 3000 N Grandview Blvd · Waukesha, WI · 53188-1615

Is this the product you have?

    • GE Healthcare
    • Dash 3000
    • Dash 4000 and Dash 5000 Patient Monitors
    • Dash Port2 Docking Station
Lot codes and dates
  • Parent SN

    2,327 of 2,327 codes

    • SBG06451608GA
    • SBG06451606GA
    • SBG06451607GA
    • SBG06451638GA
    • SBG06451605GA
    • A4EH1211G
    • A4EH1212G
    • A4EH1251G
    • A4EH1284G
    • A4EH1286G
    • A4EH1287G
    • A4EH1288G
    • A4EH1196G
    • A4EH1197G
    • A4EH1199G
    • A4EH1203G
    • A4EH1204G
    • A4EH1281G
    • A4EH1192G
    • A4EH1193G
    • A4EH1214G
    • A4EH1227G
    • A4EH1228G
    • A4EH1216GR
    • A4EH1219G
    • A4EH1220GR
    • A4EH1291G
    • A4EH1191G
    • A4EH1229G
    • A4EH1230G
    • A4EH1231G
    • A4EH1240G
    • A4EH1245GR
    • A4EH1275G
    • A4EH1264G
    • A4EH1195G
    • A4EH1246G
    • A4EH1247G
    • A4EH1267G
    • A4EH1268GR
    • A4EH1269G
    • A4EH1271G
    • A4EH1200G
    • A4EH1249G
    • A4EH1250G
    • A4EH1254G
    • A4EH1256G
    • A4EH1257G
    • A4EH1258G
    • A4EH1201G
    • A4EH1202G
    • A4EH1222G
    • A4EH1223G
    • A4EH1205G
    • A4EH1206G
    • A4EH1224G
    • A4EH1225G
    • A4EH1226G
    • A4EH3954GR
    • A4EH1356G
Amount recalled
178,711 (92,123 US, 86,588 OUS)

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

Why it was recalled

GE has become aware of multiple issues affecting the Dash 3000/4000/5000 Patient Monitor and Dash Port 2 Docking Station: DASH: 1. Dash stops communicating on the Unity Network resulting in Loss of Monitoring at the CARESCAPE" CIC Pro Central Station*. 2. Dash displays distorted ECG waveforms in combination monitoring mode. 3. Dash incorrectly becomes Time Master on the Unity Network¿. 4.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Aug 25, 2016 · Data as of Sep 19, 5:33 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.