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No image published for this recall

Nucletron b.v. Intrauterine tube

Official notice

8 Apr 2026

Last checked

8 Apr 2026

Medium riskHealth Canada

An official Health Canada notice concerns Nucletron b.v. Intrauterine tube. 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. Published 2026-04-08.

What to do now

Contact the manufacturer if you require additional information. APPLICATION.SUPPORT.NA@ELEKTA.COM TEL: +1 855 6935358 HTTPS://WWW.ELEKTA.COM

Recall number

81859

Official notice

2026-04-08

The hazard

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.

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Skus

152019-00, 152021-00, 152008-00, 152015-00, 152018-00, 152005-00, 152007-00, 152012-00, 152014-00, 152009-00, 152010-00, 152011-00, 152013-00, 152016-00, 152020-00, 152022-00, 152017-00, 152023-00, 126014-01, 126019-00, 126016-01, 126020-00, 126020-01, 126021-01, 126016-00, 126017-00, 126017-01, 126018-01, 126023-00, 126023-01, 126013-01, 126014-00, 126018-00, 126013-00, 126015-00, 126021-00, 126022-00, 126022-01, 126015-01, 126019-01

Other

RA RA-81859

Model Numbers

152019-00, 152021-00, 152008-00, 152015-00, 152018-00, 152005-00, 152007-00, 152012-00, 152014-00, 152009-00, 152010-00, 152011-00, 152013-00, 152016-00, 152020-00, 152022-00, 152017-00, 152023-00, 126014-01, 126019-00, 126016-01, 126020-00, 126020-01, 126021-01, 126016-00, 126017-00, 126017-01, 126018-01, 126023-00, 126023-01, 126013-01, 126014-00, 126018-00, 126013-00, 126015-00, 126021-00, 126022-00, 126022-01, 126015-01, 126019-01

Recall Numbers

81859

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Affected products

Product 1

Lot or serial number - Not applicable., Model or catalogue number - 152019-00

Product 2

Lot or serial number - Not applicable., Model or catalogue number - 152021-00

Product 3

Lot or serial number - Not applicable., Model or catalogue number - 152008-00

Product 4

Lot or serial number - Not applicable., Model or catalogue number - 152015-00

Product 5

Lot or serial number - Not applicable., Model or catalogue number - 152018-00

Product 6

Lot or serial number - Not applicable., Model or catalogue number - 152005-00

Product 7

Lot or serial number - Not applicable., Model or catalogue number - 152007-00

Product 8

Lot or serial number - Not applicable., Model or catalogue number - 152012-00

Product 9

Lot or serial number - Not applicable., Model or catalogue number - 152014-00

Product 10

Lot or serial number - Not applicable., Model or catalogue number - 152009-00

Product 11

Lot or serial number - Not applicable., Model or catalogue number - 152010-00

Product 12

Lot or serial number - Not applicable., Model or catalogue number - 152011-00

Product 13

Lot or serial number - Not applicable., Model or catalogue number - 152013-00

Product 14

Lot or serial number - Not applicable., Model or catalogue number - 152016-00

Product 15

Lot or serial number - Not applicable., Model or catalogue number - 152020-00

Product 16

Lot or serial number - Not applicable., Model or catalogue number - 152022-00

Product 17

Lot or serial number - Not applicable., Model or catalogue number - 152017-00

Product 18

Lot or serial number - Not applicable., Model or catalogue number - 152023-00

Product 19

Lot or serial number - Not applicable., Model or catalogue number - 126014-01

Product 20

Lot or serial number - Not applicable., Model or catalogue number - 126019-00

Product 21

Lot or serial number - Not applicable., Model or catalogue number - 126016-01

Product 22

Lot or serial number - Not applicable., Model or catalogue number - 126020-00

Product 23

Lot or serial number - Not applicable., Model or catalogue number - 126020-01

Product 24

Lot or serial number - Not applicable., Model or catalogue number - 126021-01

Product 25

Lot or serial number - Not applicable., Model or catalogue number - 126016-00

Product 26

Lot or serial number - Not applicable., Model or catalogue number - 126017-00

Product 27

Lot or serial number - Not applicable., Model or catalogue number - 126017-01

Product 28

Lot or serial number - Not applicable., Model or catalogue number - 126018-01

Product 29

Lot or serial number - Not applicable., Model or catalogue number - 126023-00

Product 30

Lot or serial number - Not applicable., Model or catalogue number - 126023-01

Product 31

Lot or serial number - Not applicable., Model or catalogue number - 126013-01

Product 32

Lot or serial number - Not applicable., Model or catalogue number - 126014-00

Product 33

Lot or serial number - Not applicable., Model or catalogue number - 126018-00

Product 34

Lot or serial number - Not applicable., Model or catalogue number - 126013-00

Product 35

Lot or serial number - Not applicable., Model or catalogue number - 126015-00

Product 36

Lot or serial number - Not applicable., Model or catalogue number - 126021-00

Product 37

Lot or serial number - Not applicable., Model or catalogue number - 126022-00

Product 38

Lot or serial number - Not applicable., Model or catalogue number - 126022-01

Product 39

Lot or serial number - Not applicable., Model or catalogue number - 126015-01

Product 40

Lot or serial number - Not applicable., Model or catalogue number - 126019-01

Risk / hazard

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.

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Nucletron B.v.

Source & status

Source

Health Canada

Tier

beta

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

81859

Classification

Type II

Source tier

beta

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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