# FDA recall Z-0195-2023

> **Avanos Medical, Inc.** · Class II · device recall initiated 2022-09-14.

## 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 for recall

Sterile extension sets were distributed without an expiration date

## Distribution

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

## Key facts

- **Recall number:** Z-0195-2023
- **Recalling firm:** Avanos Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-09-14
- **Report date:** 2022-11-16
- **Termination date:** 2023-08-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Alpharetta, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0195-2023

## Citation

> AI Analytics. FDA recall Z-0195-2023. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-0195-2023. Source: US FDA. Licensed CC0.

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