# FDA recall Z-2322-2019

> **Becton Dickinson & Co.** · Class II · device recall initiated 2019-07-17.

## Product

Kit BD Max Cdiff EU;  Catalog # 442555

## Reason for recall

The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.

## Distribution

AL, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MT, NC, NH, NJ, NM, NV, NY, OH, OR, PA, PR, RI, SC, TN, TX, VA, WA, WI, WV    Worldwide: Australia, Belgium, Brazil, Canada, Chile, China, Hong Kong, Japan, Korea, Mexico, Singapore, Taiwan

## Key facts

- **Recall number:** Z-2322-2019
- **Recalling firm:** Becton Dickinson & Co.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-07-17
- **Report date:** 2019-08-28
- **Termination date:** 2020-05-13

- **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-2322-2019

## Citation

> AI Analytics. FDA recall Z-2322-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2322-2019. Source: US FDA. Licensed CC0.

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