Nucletron B.V. Intrauterine Tube Recall - Tip Detachment
Summary
Health Canada issued a Type II medical device recall for Nucletron B.V. Intrauterine Tubes (catalog numbers 152019-00 through 126015-01) affecting 44 product lots. The recall addresses a safety concern where the tip of the 4mm diameter IU tube detached and remained within a patient during use. Healthcare providers should contact the manufacturer for additional information.
What changed
Health Canada issued a Type II medical device recall for Nucletron B.V. Intrauterine Tubes, affecting 44 catalog numbers (152019-00 through 126015-01). The safety concern involves the detachment of the tip of the 4mm diameter IU tube that remained within a patient during a medical procedure.
Healthcare providers should contact the manufacturer at the provided email or phone number for additional information and guidance.
What to do next
- Contact manufacturer at APPLICATION.SUPPORT.NA@ELEKTA.COM or 1-855-693-5358 for additional information
- Follow any manufacturer instructions regarding affected devices
Archived snapshot
Apr 9, 2026GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.
Health product recall
Nucletron B.V. Intrauterine Tube
Brand(s)
Last updated
2026-04-08
Summary
Product Nucletron B.V. Intrauterine Tube Issue Medical devices - Performance What to do Contact the manufacturer if you require additional information.
APPLICATION.SUPPORT.NA@ELEKTA.COM
TEL: +1 855 6935358
HTTPS://WWW.ELEKTA.COM
Audience Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Intrauterine Tube | Not applicable. | 152019-00 |
| Intrauterine Tube | Not applicable. | 152021-00 |
| Intrauterine Tube | Not applicable. | 152008-00 |
| Intrauterine Tube | Not applicable. | 152015-00 |
| Intrauterine Tube | Not applicable. | 152018-00 |
| Intrauterine Tube | Not applicable. | 152005-00 |
| Intrauterine Tube | Not applicable. | 152007-00 |
| Intrauterine Tube | Not applicable. | 152012-00 |
| Intrauterine Tube | Not applicable. | 152014-00 |
| Intrauterine Tube | Not applicable. | 152009-00 |
| Intrauterine Tube | Not applicable. | 152010-00 |
| Intrauterine Tube | Not applicable. | 152011-00 |
| Intrauterine Tube | Not applicable. | 152013-00 |
| Intrauterine Tube | Not applicable. | 152016-00 |
| Intrauterine Tube | Not applicable. | 152020-00 |
| Intrauterine Tube | Not applicable. | 152022-00 |
| Intrauterine Tube | Not applicable. | 152017-00 |
| Intrauterine Tube | Not applicable. | 152023-00 |
| Intrauterine Tube | Not applicable. | 126014-01 |
| Intrauterine Tube | Not applicable. | 126019-00 |
| Intrauterine Tube | Not applicable. | 126016-01 |
| Intrauterine Tube | Not applicable. | 126020-00 |
| Intrauterine Tube | Not applicable. | 126020-01 |
| Intrauterine Tube | Not applicable. | 126021-01 |
| Intrauterine Tube | Not applicable. | 126016-00 |
| Intrauterine Tube | Not applicable. | 126017-00 |
| Intrauterine Tube | Not applicable. | 126017-01 |
| Intrauterine Tube | Not applicable. | 126018-01 |
| Intrauterine Tube | Not applicable. | 126023-00 |
| Intrauterine Tube | Not applicable. | 126023-01 |
| Intrauterine Tube | Not applicable. | 126013-01 |
| Intrauterine Tube | Not applicable. | 126014-00 |
| Intrauterine Tube | Not applicable. | 126018-00 |
| Intrauterine Tube | Not applicable. | 126013-00 |
| Intrauterine Tube | Not applicable. | 126015-00 |
| Intrauterine Tube | Not applicable. | 126021-00 |
| Intrauterine Tube | Not applicable. | 126022-00 |
| Intrauterine Tube | Not applicable. | 126022-01 |
| Intrauterine Tube | Not applicable. | 126015-01 |
| Intrauterine Tube | Not applicable. | 126019-01 |
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.
Additional information
Details
Original published date:
2026-04-08
Alert / recall type Health product recall Category Health products - Medical devices - Radiology Companies Nucletron B.V.
Waardgelder 1, Veenendaal, Netherlands, 3905 TH
Published by Health Canada Audience Healthcare Recall class Type II Recall date
2026-03-20
Identification number RA-81859
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Source
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