FDA Device recall Z-3166-2026
Centricity Enterprise Archive V2, V3, and V4, software product for receiving, archiving, and sending electronic medical data, All Versions
- FDA Device
- Class II
- ongoing
- Published 2026-09-23
On 2026-09-23 the FDA classified a Class II recall of Centricity Enterprise Archive V2, V3, and V4, software product for receiving, archiving, and sending electronic medical data, All Versions by Ge Healthcare, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3166-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-07-31 |
| Published | 2026-09-23 |
| Last updated | 2026-09-29 05:30 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
Centricity Enterprise Archive V2, V3, and V4, software product for receiving, archiving, and sending electronic medical data, All Versions
Reason
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.
Identifiers
| code_info | UDI-DI: V4 - 00840682102766; System IDs: CARTI02312615 CARTI22225617 520784EASFTW1 19233337_EA MARICOPAC02308032 602406…UDI-DI: V4 - 00840682102766; System IDs: CARTI02312615 CARTI22225617 520784EASFTW1 19233337_EA MARICOPAC02308032 602406SAEAFSW 602997SAEASW-24 SVRHC14765622 520458CVEASW 520780SAEASW 520784EASSASW 520629EA1 BERMUDACA02257222 BERMUDACA02257223GW ASHPACSEA1P 805395EASW PMHD15081203 805725EASW1 V5SPORTS01804915 559582CAEASW 760775CAEASW 310673CAPACSSW UHVNAEAPRD01 UHEAVNATEST01 UHVNAEAPRD02 UHVNAEAPRD03 UHVNAEAPRD04 UHVNAEAPRD05 UHVNAEAPRD06 310349EASW1 310349EASW2 310349EASW3 310ODCEASW4 ADVENTIST02256061 323726CAEASW NDMGCAWEB PALMDALEM02354935 PALMDALEM19604722 PALMDALEM19604723 661948ISBSW 818676EA01 916781MMBSW1 916781MMBSW2 ADVENTIST1474489 SUTH20087395 707554EASW 916733EASTSW1 916733EASTSW2 916733EASTSW3 916733EASTSW4 916733EASTSW5 916733EASW2 916733EASW3 916733EASW4 916733EASW5 916733SAEASW SUTH20992909 SUTH20992910 SUTH20992912 SUTH20992914 650696EASW 408590EAAIMSW 805542SAEASW VSMY01820424 VCM01983687 SONORAREG26747425 RANCHO02255035 RANCHOTEA01 RANCHODTEA01 UHS24494273 VCM01819 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-29 05:30 UTC. Current status: ongoing.
Other recalls by Ge Healthcare
- Centricity PACS V2, V3, V4, V6, V7, software product is intended for the storage, reading, diagnostic review, analysis, annotation, distrib…
FDA Device · Class II · 2026-09-23 · Ge Healthcare - Workflow Core Services V8, intended to provide set of services for storage and retrieval of patient data, exams and performs system Adminis…
FDA Device · Class II · 2026-09-23 · Ge Healthcare - Core Services Hub V8, a set of backend services including Cross Enterprise (XE) and Workflow Core (WFC) services that enables enterprise im…
FDA Device · Class II · 2026-09-23 · Ge Healthcare - Enterprise Archive V8, software product for receiving, archiving, and sending electronic medical data, All versions
FDA Device · Class II · 2026-09-23 · Ge Healthcare - Centricity PACS Server V7, intended for managing digital medical images and associated data, All versions
FDA Device · Class II · 2026-09-23 · Ge Healthcare
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3166-2026%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.