Public recall detail

Nucletron B.V. Intrauterine Tube

2026-04-08

medium
Radiology Performance
Quick summary

Quick summary: Nucletron B.V. Intrauterine Tube. Reason: Performance. Category: Radiology. Date: 2026-04-08.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Nucletron B.V. Intrauterine Tube. Reason: Performance. Category: Radiology. Date: 2026-04-08.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandNucletron B.V.
ProductNucletron B.V. Intrauterine Tube
IssueMedical devices - Performance
Recall classType II
IdentificationRA-81859

Affected products

ProductIntrauterine Tube
LotNot applicable.
Model152019-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152021-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152008-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152015-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152018-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152005-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152007-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152012-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152014-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152009-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152010-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152011-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152013-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152016-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152020-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152022-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152017-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model152023-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126014-01
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126019-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126016-01
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126020-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126020-01
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126021-01
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126016-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126017-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126017-01
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126018-01
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126023-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126023-01
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126013-01
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126014-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126018-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126013-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126015-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126021-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126022-00
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126022-01
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126015-01
Serial numberNot applicable.
DescriptionIntrauterine Tube
ProductIntrauterine Tube
LotNot applicable.
Model126019-01
Serial numberNot applicable.
DescriptionIntrauterine Tube

Issue

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.

What you should do

  • Contact the manufacturer if you require additional information. APPLICATION.SUPPORT.NA@ELEKTA.COM TEL: +1 855 6935358 HTTPS://WWW.ELEKTA.COM
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Radiology
CompaniesNucletron B.V. Waardgelder 1, Veenendaal, Netherlands, 3905 TH
Recall date2026-03-20
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-81859
Background{}
CompaniesNucletron B.V. Waardgelder 1, Veenendaal, Netherlands, 3905 TH
AudiencesHealthcare
Source updated2026-04-08

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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