# FDA recall Z-0110-2024

> **Becton Dickinson & Co.** · Class II · device recall initiated 2023-09-12.

## Product

BD BACTEC Plus Aerobic/F Culture Vials, Catalog Number 442023

## Reason for recall

Certain vials of the BD BACTEC" Plus Aerobic/F Culture Vials have a labeling issue where duplicate barcode sequence numbers have been identified on more than one vial.

## Distribution

Worldwide - US Nationwide distribution.

## Key facts

- **Recall number:** Z-0110-2024
- **Recalling firm:** Becton Dickinson & Co.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-12
- **Report date:** 2023-10-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Sparks, MD, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0110-2024

## Citation

> AI Analytics. FDA recall Z-0110-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0110-2024. Source: US FDA. Licensed CC0.

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