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Symbia Pro.specta Q3 11364751Recalls & reported problems

Siemens Medical Solutions USA, Inc. · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

  1. Jul 12, 2023Class IIOpen, Classified

    During a whole-body planar scan with auto-contour, there is a possibility the short-linear drive (SLD) look-ahead sensors may trigger earlier than expected and may result in detector 1 positioning further from the patient than needed leading to a reduction in image resolution.

    Z-2256-2023 · Root cause: Device Design · Recall details · FDA record ↗

Other System, tomography, computed, emission devices

All System, tomography, computed, emission devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page