# FDA recall Z-2035-2024

> **Avanos Medical, Inc.** · Class III · device recall initiated 2024-03-04.

## Product

NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product descriptions:     a. 0.5mL Oral Syringe Amber NonSterile, Product Code BA-S05EO;   b. 12mL Oral Syringe Amber NonSterile, Product Code BA-S12EO;   c. 1mL Oral Syringe Amber NonSterile, Product Code BA-S1EO;   d. 20mL Oral Syringe Amber NonSterile, Product Code BA-S20EO;   e. 35mL Oral Syringe Amber NonSterile, Product Code BA-S35EO;   f. 3mL Oral Syringe Amber NonSterile, Product Code BA-S3EO;   g. 60mL Oral Syringe Amber NonSterile, Product Code BA-S60EO;   h. 6mL Oral Syringe Amber NonSterile, Product Code BA-S6EO;

## Reason for recall

The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.

## Distribution

Worldwide distribution - US Nationwide and the countries of Australia, New Zealand, Canada, Switzerland, Netherlands, Singapore.

## Key facts

- **Recall number:** Z-2035-2024
- **Recalling firm:** Avanos Medical, Inc.
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-03-04
- **Report date:** 2024-06-19

- **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-2035-2024

## Citation

> AI Analytics. FDA recall Z-2035-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-2035-2024. Source: US FDA. Licensed CC0.

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