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Geneva 152019-00Recalls & reported problems

Nucletron B.V. · Intrauterine Tube 30mm 45° · Class 2

All models of Geneva (17)

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. Apr 3, 2026Class IIOpen, Classified

    Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.

    Z-2712-2026 · Root cause: Process control · Recall details · FDA record ↗

Other System, applicator, radionuclide, remote-controlled devices

All System, applicator, radionuclide, remote-controlled devices →

Sources and updates

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