Skip to content

GenevaRecalls & reported problems across all models

Nucletron B.V. · 17 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

1 open recall names at least one Geneva model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

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

We found 17 models of Geneva by Nucletron B.V. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

1 FDA recall record name at least one of these models by its device 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Geneva recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

  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 · names 17 of these models · Recall details · FDA record ↗

Geneva models

17 models, most reported first. Each model has its own page with its reports, recalls and device details.

Other Nucletron B.V. products

All Nucletron B.V. devices →

Sources and updates

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