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FDA Device recall Z-3286-2026

Positron Emission Tomography and Computed Tomography System, Model: uMI Panvivo with software

On 2026-10-07 the FDA classified a Class II recall of Positron Emission Tomography and Computed Tomography System, Model: uMI Panvivo with software by Shanghai United Imaging Healthcare, citing positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-3286-2026
ClassificationClass II
Statusongoing
Initiated2026-08-11
Published2026-10-07
Last updated2026-10-13 05:30 UTC
CompanyShanghai United Imaging Healthcare
DistributionUS

Product

Positron Emission Tomography and Computed Tomography System, Model: uMI Panvivo with software

Reason

Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.

Identifiers

code_infoUDI-DI: 06971576832231. Serial Number/Software: 11MI500004/R002.4.0.1872339, 11MI500005/R002.4.0.1872339, 11MI500006/R002.4.0.1872339

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-10-13 05:30 UTC. Current status: ongoing.

Other recalls by Shanghai United Imaging Healthcare

All Shanghai United Imaging Healthcare recalls

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3286-2026%22

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