---
title: "Artoura Breast Tissue Expanders Reference Numbers: SDC-100H SDC-110H SDC-120H... — FDA record Z-1686-2026 | Is It on Recall"
description: "Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break."
url: https://isitonrecall.com/recall/fda-device-z-1686-2026-artoura-breast-tissue-expanders-reference-numbers-sdc-100h-sdc-110h-sdc-120h-sdc-130h-sdc-135h-sdc-1/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Artoura Breast Tissue Expanders Reference Numbers: SDC-100H SDC-110H SDC-120H SDC-130H SDC-135H SDC-140H SDC-150H SDC... — FDA record Z-1686-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Feb 18, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Artoura Breast Tissue Expanders Reference Numbers: SDC-100H SDC-110H SDC-120H SDC-130H SDC-135H SDC-140H SDC-150H SDC-155H Smooth High Profile Tissue Expander, 225cc, 300cc, 375cc, 475cc, 500cc, 600cc, 750cc, 850cc
- **Reason**: Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
- **Classification**: Class II
- **Recalling firm**: Mentor Texas, LP.
- **Quantity**: Not supplied
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1686-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1686-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI(s): 10081317028168 10081317028175 10081317028199 10081317028243 10081317028250 10081317028267 10081317028274 10081317028151 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Albania, Australia, Austria, Belgium, Bulgaria, Croatia, Denmark, Finland, France, Germany, Iceland, Ireland, Italy, Norway, Pakistan, Poland, Romania, Saudi Arabia, Singapore, Slovakia, Slovenia, Spain, Sweden, Switzerland, Taiwan, United Kingdom, Czech Republic.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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- [Kentucky](https://isitonrecall.com/state/kentucky/)
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- [Maryland](https://isitonrecall.com/state/maryland/)
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- [Nevada](https://isitonrecall.com/state/nevada/)
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- [Ohio](https://isitonrecall.com/state/ohio/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Apr 8, 2026
- **Recall initiation date**: Feb 18, 2026
- **Center classification date**: Mar 27, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1686-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Mentor Texas, LP. records](https://isitonrecall.com/brand/mentor-texas-lp/)
