RecallRadar

FDA Device recall Z-3280-2026

Computed Tomography X-ray System, Model: uCT 780 with software

On 2026-10-07 the FDA classified a Class II recall of Computed Tomography X-ray System, Model: uCT 780 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-3280-2026
ClassificationClass II
Statusongoing
Initiated2026-08-11
Published2026-10-07
Last updated2026-10-13 05:30 UTC
CompanyShanghai United Imaging Healthcare
DistributionUS

Product

Computed Tomography X-ray System, Model: uCT 780 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_info
UDI-DI: 06971576831050. Serial Number/Software: 684001/R001.17.6.1607336-Re3100SP4, 684002/R001.17.6.1607336-Re3100S…UDI-DI: 06971576831050. Serial Number/Software: 684001/R001.17.6.1607336-Re3100SP4, 684002/R001.17.6.1607336-Re3100SP4, 684003/R003.8.4.1810621-Re3300SP1H1_P3, 684004/R003.8.4.1810621-Re3300SP1H1_P3, 684005/R003.8.4.1810621-Re3300SP1H1_P3, 684006/R003.8.4.1810621-Re3300SP1H1_P3, 684007/R003.8.4.1810621-Re3300SP1H1_P3, 684008/R003.8.4.1810621-Re3300SP1H1_P3, 684009/R003.8.4.1810621-Re3300SP1H1_P3, 684010/R003.8.4.1810621-Re3300SP1H1_P3, 684011/R003.8.4.1810621-Re3300SP1H1_P3, 684012/R003.9.0.1776134-Re-3300SP2, 684013/R003.11.0.1897081-Re3310SP1, 684014/R003.11.0.1897081-Re3310SP1

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-3280-2026%22

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