FDA Device recall Z-3168-2026
Centricity PACS V2, V3, V4, V6, V7, software product is intended for the storage, reading, diagnostic review, analysis, annotation, distrib…
- FDA Device
- Class II
- ongoing
- Published 2026-09-23
On 2026-09-23 the FDA classified a Class II recall of Centricity PACS V2, V3, V4, V6, V7, software product is intended for the storage, reading, diagnostic review, analysis, annotation, distrib… 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-3168-2026 |
| 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 PACS V2, V3, V4, V6, V7, software product is intended for the storage, reading, diagnostic review, analysis, annotation, distribution, printing, editing, and processing of digital images and data acquired from diagnostic imaging devices, 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 - 00840682124430, V6 - 00840682104807, V7 - 00840682145572; System IDs: CARTI02312611 CARTI22214087T 928757V…UDI-DI: V4 - 00840682124430, V6 - 00840682104807, V7 - 00840682145572; System IDs: CARTI02312611 CARTI22214087T 928757VPASW 928757VPBSW 602344PVSW2 602344REPSITEB MARICOPAC02308029 602344TIMSVM 441236VPSW 805395PVSW 805395PVTSW 310349PACSSWPV UCLAMC2259090 310349PACSSWBPV UCLAMC2259063 916781CPACSSRWT PALMDALEM01810792 PALMDALEM16023955 PALMDALEM20508297 909788HCAPACS1 916781CPACSCKS 916781CPACSBCKS GSHCACPSW GSH320037250 GSHCACTPSW RANCHO02255039 RANCHOPISU2 RANCHOPTESTISU 805370HCALR VMPACS69 LOSROBLES19666790 MCANPACSW CENPACSW 303584HCAPVSW 303584REPBSW 303584HCAPVSWTESTIMS 970476PVSW VVMC15111181 VVMC27255473 302674PACSSW 302674PACSBSW 302736SAEATSW JFKSW JFKR19980220B JFKSWOPT 727462PVSW 727462PVBSW MPMH2259089T 772461HCAPACSW 772461HCAPACSW1 772461HCAPACSWT 352333PACSSW NFRH19663978B 904202BMCDSW 904202BMCSSW 904202BMCDTSW MH826898334 407518COREPACS 407518CPREPB KRMCOREPACSSW KRMC19478073 KRMC25216192 615344HCASW PCMC420084442 WFLHIV01 WESTFLORI19661467 772335PACSSW 772335PVSW 8 |
|---|
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
- 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 Enterprise Archive V2, V3, and V4, 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-3168-2026%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.