PlainRecalls

Nucletron Bv

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Jan 8, 2020

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Agency notice ledger

Federal filing book Nucletron Bv LIGHT-BOOK · SINGLE-AGENCY

#5,450 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,450 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jan 8, 2020
  • PHOTO 3M Company

Nearest notice-volume peer: 3M Company (0 notice gap)

Nucletron Bv accounts for about 0.002% of the 104,423-notice archive on 2 distinct filings — a light share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Nucletron Bv sits among 14,151 recalling firms

Nucletron Bv ranks 5,450th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Nucletron Bv vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

2 5450th of 14151 higher than 8,037 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Nucletron Bv in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Nucletron Bv holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jan 8, 2020

There is a complaint regarding internal check cable guide mechanism failure for the Nucletron Flexitron brachytherapy afterloader system. Due to an obstruction during the check cable out drive, the internal guiding tube became displaced and the check cable became damaged. This issue could cause treatment interruption or in a very unlikely scenario, incorrect source positioning and radiation treatment errors.
FDA Devices Moderate Nov 1, 2017

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 radiation treatments in three dimensions for the purpose of treating patients with cancer. The treatment plans provide estimates of dose distributions expected during the proposed treatment and may be used to administer treatments after review and approval by qualified medical personnel.

Nucletron Bv is a small archive contributor

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

3M Company 2 3M Company/3m Espe Dental Products 2 A.o. Smith Electrical Products Co., of Tipp City, Ohio 2 Abbott GmbH 2

Frequently Asked Questions

How many federal recall notices name Nucletron Bv? ▼
PlainRecalls indexes 2 distinct federal recall events naming Nucletron Bv, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Nucletron Bv sit among other recalling firms? ▼
Nucletron Bv ranks #5,450 of 14,151 by distinct recall-event count among 14,151 firms in this archive (57th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Nucletron Bv's notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Nucletron Bv's filing book? ▼
Filings for Nucletron Bv span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Nucletron Bv: 2 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Nucletron Bv; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026