Enterprise Archive V8, software product for receiving, archiving, and sending electronic medical data, All…
Medical device recall Z-3167-2026. Published in FDA’s Enforcement Report on Sep 23, 2026.
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 Sep 23, 2026. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 1298 systems 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?
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Enterprise Archive V8, software product for receiving, archiving, and sending electronic medical data, All versions
1298 systems, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
UDI-DI: V4 - 00195278409287; System IDs: BIRMINGHAM20886386 SevierCou21180101 SevierCou21180111 UOAR24851211 UOAR23214501 CARTI27326017 KGM21766613T KGM21332085 KGM21677289 HRH323169307 HONORHEALT21179400 MIHS25042933 MIHS25151161…
Every code shown here, 1,975 characters
UDI-DI: V4 - 00195278409287; System IDs: BIRMINGHAM20886386 SevierCou21180101 SevierCou21180111 UOAR24851211 UOAR23214501 CARTI27326017 KGM21766613T KGM21332085 KGM21677289 HRH323169307 HONORHEALT21179400 MIHS25042933 MIHS25151161 MIHS25042933 MIHS25151165 MIHS25151166 ADHR27301883 PMIO26874972 PMHD27236488 PIPELINEH26974662 PIPELINEH27011598 SANFERNAN23238694 KRM22180898 MHL23269965 SUTH26668887 NORV21741298 24931893EdgeEA 25083358StgEdgeEA VCM27268846 SCRL24283967 SCRL23202147 SFGH24285530 USHC25292971 USHC26580362 GSH321314340 LosRobles23253832 QTHBL26325570 DENVERVA21733821 DENVER VA24406115 BOULDER22107026 BOULDER22107318 BOULDERCO24954910 HHL27121414 Not Available GRHD20869082A GRHD20869563B GRHD20870041T GRHD27231932 Not Available VVMC21290279 VVMC24397815 VVMC23203058 DDOC26923413 BAYHEALTH22212474 BAYHEALTH23201150 BAYHEALTHxxx BAYHEALTH26871762 JFKR20875123CEAGW 100029-1-Enterprise Archive-27124494 106428-3-Enterprise Archive-21313581 BYH24954908 BYH26856929 BYH26856932 LMC421600077 MH820838229 BIHT21020972 BIHT21305845 BIHT21305846 BIHT21305854 BIHT21305855 BIHT21305856 BIHT21310361 MH826770189 KRMC22464526 KRMC23157942 OFMC22161730T OFMC23066623P ORDC20944523 ORDC21315028 WELLINGTON27007867 RMCB23599904 PALMBEACH26587094 PALMBEACH26668888 AMCL21358642 CRMC21017209 HLEEMOFF21248284 HLEEMOFF21248387 HLEEMOFF21248397 BYH26649265 BYH26705437 BYH26782652 BYH26782654 WELLINGTON24453857 WELLINGTON24608353T LAKESIDEM21200034 LAKESIDEM21728988 WELLINGTON NEUROSKEL22629459 FLMC24438811EAT FLMC23269954EAP MRMC220924398 106590-2-Enterprise Archive-21847158 MRMC221300605 MRMC221300647T TRMCN25042932 106590-2-Enterprise Archive-25310918 MRMC226735314 MH826900860 SGHS21166828 SGHS21174955S SGHS24386768 106684-1-Enterprise Archive-23253823 ICA27062092 WHSS24437725 WHSS23208965 CWVM26790668 EID23167355 UIMC21180577EA1 UIMC21180577EA2 JHSJHOCC24505032 JHSJHOCC24509247 TUCM25188743 TUCM25191960 ULHH26814916 RPS27317305 LaitekDataMigrationETPLab1EA…
FDA’s list runs to 20,130 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 - US Nationwide distribution.
These words name no state.
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?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, 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 Jul 31, 2026.
- FDA classified it on Sep 15, 2026.
- FDA’s Enforcement Report published it on Sep 23, 2026.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- GE Healthcare, of Chicago, IL.
- 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 20,130 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
-
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.