Product Wiki · Recalls · Health Canada — Medical Devices

Nucletron B.V. Intrauterine Tube — recall 81859

Health Canada — Medical Devices · Canada · 2026-04-08 · Type II

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
81859
Date of alert
2026-04-08
Country / jurisdiction
Canada
Authority classification
Type II
Notice type
recall
Product category
Radiology
Product type
Medical devices
Reported risk: Elekta are informing customers of a safety concern regarding the detachment of the tip of the Intrauterine Tube (IU tube) with a 4mm diameter that remained within a patient.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/nucletron-bv-intrauterine-tube

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.