---
title: "Y-CONNECTOR: 6\" Small Kink Resistant Tubing Bifurcated Connector /2 Male Luer... — FDA record Z-0195-2023 | Is It on Recall"
description: "Sterile extension sets were distributed without an expiration date"
url: https://isitonrecall.com/recall/fda-device-z-0195-2023-y-connector-6-small-kink-resistant-tubing-bifurcated-connector-2-male-luer-locks-1-female-luer-lock/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Y-CONNECTOR: 6" Small Kink Resistant Tubing Bifurcated Connector /2 Male Luer Locks, 1 Female Luer Lock, Labeled as: ... — FDA record Z-0195-2023

Reported terminated

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 Sep 14, 2022. 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**: Y-CONNECTOR: 6" Small Kink Resistant Tubing Bifurcated Connector /2 Male Luer Locks, 1 Female Luer Lock, Labeled as: SUMMIT MEDICAL PRODUCTS, REF 220227; MPS Acacia CAT NO: BC-006-04; MEDICAL PRODUCTS SPECIALISTS EXTENSION SET, Catalog Number BC00604, pain control pump accessory
- **Reason**: Sterile extension sets were distributed without an expiration date
- **Classification**: Class II
- **Recalling firm**: Avanos Medical, Inc.
- **Quantity**: 1378 units
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0195-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0195-2023%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 | ALL LOT CODES |

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

## Distribution

US: CA, CO, FL, MI, NM, OH, OR, TN, TX, UT, WI

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

- [California](https://isitonrecall.com/state/california/)
- [Colorado](https://isitonrecall.com/state/colorado/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Michigan](https://isitonrecall.com/state/michigan/)
- [New Mexico](https://isitonrecall.com/state/new-mexico/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Oregon](https://isitonrecall.com/state/oregon/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Utah](https://isitonrecall.com/state/utah/)
- [Wisconsin](https://isitonrecall.com/state/wisconsin/)

## Dates in the source

- **Report date**: Nov 16, 2022
- **Recall initiation date**: Sep 14, 2022
- **Center classification date**: Nov 7, 2022
- **Termination date**: Aug 31, 2023

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-0195-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Avanos Medical, Inc. records](https://isitonrecall.com/brand/avanos-medical-inc/)