FDA Medical devices recall ·
Centricity PACS V2, V3, V4, V6, V7, software product is intended for the… recall
- Recall number
- Z-3168-2026
- Date
- (initiated July 31, 2026)
- Company / brand
- GE Healthcare
500 W Monroe St, Chicago, IL, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 1443 systems
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
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
Why was it recalled?
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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
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 850875PVSW2 904819PVSW 904819PV2SW 904819PVTSW 727519PVBSW 850325PACSCORE CRMC820084433 888663CPBSW 727519PVSW 888663CPTSW 888663CPB2SW 727519PVTSW VAMAF02345966 727519PVTSW-MOCK 407518SCPACSHC 850325HCASWOPT WFLHIVT01 PCMC42259036 352333PACSTSW WELLINGTON01810730 WELLINGTON19678279T WELLINGTON20036598 MJPACSW TRMPACSW TRMNC20021605 100115-8-Centricity PACS-21222171 TRMTESTPACS Doctors Ho22222417 MJPACDRSW 706651HCACORE 912466PVSW SGHS2259039 912276PVSW 912276PVTSW 706278PACSSWPV 706278PACSSWBPV
Distribution
Worldwide - US Nationwide distribution.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-3168-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.