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Geneva 152014-00Recalls & reported problems

Nucletron B.V. · Intrauterine Tube 40mm 30° · Class 2

Data updated Oct 13, 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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Apr 3, 2026Open, 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 · FDA record ↗

Other System, applicator, radionuclide, remote-controlled devices

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

Sources and updates

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