Skip to content

Definium Tempo ProRecalls & reported problems

GE Hualun Medical Systems Co., Ltd · Definium Tempo Pro System UDI · Class 2

All models of Definium (3)

Data updated Oct 16, 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 16, 2026.

Recalls naming this device

  1. Jan 28, 2025Open, Classified

    The user can continue to take the next exposure after reaching the Automatic Exposure Control (AEC) limit, without taking any further actions to acknowledge or adjust exposure techniques. In all cases, a message still appears on the screen when the AEC limit is reached.

    Z-1045-2025 · Root cause: Radiation Control for Health and Safety Act · Recall details · FDA record ↗

Other Solid state x-ray imager (flat panel/digital imager) devices

All Solid state x-ray imager (flat panel/digital imager) devices →

Sources and updates

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