GE Healthcare, Dash Port 2 Docking Station
Medical device recall Z-0814-2013. Published in FDA’s Enforcement Report on Feb 20, 2013.
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 Feb 20, 2013. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word, and 1 state named
- 10,497 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?
GE has become aware of multiple issues affecting the Dash 3000/4000/5000 and DashPort 2 monitor. This report of correction encompasses the DashPort 2 device, in which the DashPort 2 stops communicating with the Dash, resulting in Loss of Monitoring at the CIC. The DashPort 2 status LEDs in the back of the unit indicate Unity Network and DashPort 2 to Dash communication has stopped.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
GE Healthcare, Dash Port 2 Docking Station. Product Usage: is a docking station (quick mount/dismount base) for a Dash patient monitor. The system is to monitor physiologic parameter data on adult, pediatric, and neonatal patients.
10,497, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Mfg Lot or Serial # SE507460028GA SE507460050GA SE507460053GA SE507460054GA SE507460055GA SE507460056GA SE507460057GA SE507460058GA SE507460059GA SE507460060GA SE507460061GA SE507460062GA SE507460063GA SE507460066GA SE507460067GA…
Every code shown here, 1,994 characters
Mfg Lot or Serial # SE507460028GA SE507460050GA SE507460053GA SE507460054GA SE507460055GA SE507460056GA SE507460057GA SE507460058GA SE507460059GA SE507460060GA SE507460061GA SE507460062GA SE507460063GA SE507460066GA SE507460067GA SE507480070GA SE507480071GA SE507480073GA SE507480075GA SE507480077GA SE507480078GA SE507480079GA SE507480080GA SE507480082GA SE507480083GA SE507480084GA SE507480085GA SE507480091GA SE507480098GA SE507480099GA SE507480101GA SE507480102GA SE507480105GA SE507480108GA SE507480109GA SE507480110GA SE507480115GA SE507480118GA SE507480120GA SE507480123GA SE507480124GA SE507480125GA SE507480135GA SE507480139GA SE507480148GA SE507480163GA SE507480168GA SE507480178GA SE507480185GA SE507480191GA SE507480192GA SE507480196GA SE507480197GA SE507480198GA SE507480201GA SE507480213GA SE507480217GA SE507480222GA SE507480225GA SE507480226GA SE507480230GA SE507480233GA SE507480234GA SE507480237GA SE507480245GA SE507480246GA SE507480247GA SE507480248GA SE507480250GA SE507480251GA SE507480256GA SE507480257GA SE507480258GA SE507480259GA SE507480260GA SE507480264GA SE507480268GA SE507480269GA SE507480274GA SE507480282GA SE507480289GA SE507480294GA SE507490301GA SE507490306GA SE507490308GA SE507490310GA SE507490312GA SE507490313GA SE507490314GA SE507490317GA SE507490319GA SE507490322GA SE507490323GA SE507490324GA SE507490326GA SE507490329GA SE507490331GA SE507490334GA SE507490337GA SE507490340GA SE507490341GA SE507490342GA SE507490343GA SE507490345GA SE507490385GA SE507490386GA SE507490387GA SE507490388GA SE507490389GA SE507490390GA SE507490391GA SE507490392GA SE507490393GA SE507490394GA SE507490395GA SE507490396GA SE507490397GA SE507490398GA SE507490399GA SE507490400GA SE507490401GA SE507490402GA SE507490403GA SE507490404GA SE507490405GA SE507490406GA SE507490407GA SE507490414GA SE507490419GA SE507490420GA SE507490421GA SE507490422GA SE507490423GA SE507490425GA SE507490432GA SE507490433GA SE507490435GA SE507490437GA SE507490439GA SE507490440GA SE507490446GA…
FDA’s list runs to 155,040 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 and US (nationwide) including DC and the countries of ALGERIA, ARAB EMIRATES, AUSTRALIA, AUSTRIA, BANGLADESH, BELGIUM, BRAZIL, CANADA, CHINA, CYPRUS, CZECH REPUBLIC, DENMARK, EGYPT, FRANCE, GERMANY, INDIA, ISRAEL, ITA LY, JAPAN, JORDAN, KUWAIT, MOROCCO, NETHERLANDS, NEW ZEALAND, NORWAY, POLAND, PORTUGAL, RUSSIA, SAUDI ARABIA, SINGAPORE SLOVENIA, SOUTH KOREA, SPAIN SWEDEN SWITZERLAND, TAIWAN, TURKEY, UNITED KINGDOM.
The states and territories these words name
- District of Columbia
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
The words say it went outside the United States too.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
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 Jun 13, 2012.
- FDA classified it on Feb 13, 2013.
- FDA’s Enforcement Report published it on Feb 20, 2013.
- FDA terminated it on Aug 25, 2016.
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.
- How the firm first told its customers: Letter.
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 155,040 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.