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NA Oncentra BrachyRecalls & reported problems

Nucletron B.V. · Oncentra Brachy v4.5 · Class 2

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

2 open recalls name 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
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 still open.

1 other recall cover devices cleared under the same FDA submission (K132816); 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Recalls naming this device

  1. Dec 5, 2022Open, Classified

    A reconstruction error may occur when using the Catheter Bending functionality in Applicator Modeling or Implant Modeling

    Z-0719-2023 · Root cause: Software design · Recall details · FDA record ↗

  2. Oct 13, 2021Open, Classified

    Under certain circumstances, there can be a difference between the planned and delivered dose of the two ovoid channels.

    Z-0182-2022 · Root cause: Software design · Recall details · FDA record ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K132816. One submission often covers many models, so check the product and lot details in each record.

  • Z-0050-2018 · Aug 10, 2017 · Terminated
    Oncentra Brachy 4.5 radiation therapy software The firm name on the label is Nucletron B.V. Oncentra is a radiation therapy planning software designed to analyze and plan radiati

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Sources and updates

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