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Definium Pace SelectRecalls & reported problems

GE Hualun Medical Systems Co., Ltd · Definium Pace Select system designated medical device · Class 2

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.

1 other recall cover devices cleared under the same FDA submission (K231892); they may or may not involve this specific model.

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. How this data works · Data updated Oct 13, 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-1046-2025 · Root cause: Radiation Control for Health and Safety Act · FDA record ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K231892. One submission often covers many models, so check the product and lot details in each record.

  • Z-1043-2025 · Jan 28, 2025 · Open, Classified
    Definium 656HD & Discovery XR656HD (GTINs: 00840682138598, 00195278840226, 00840682136709). X-Ray imaging system.

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

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

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.