# FDA recall Z-0193-2020

> **Becton Dickinson & Company** · Class II · device recall initiated 2019-07-31.

## Product

BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder   Catalog number 368356 - Product Usage: This product is designed to provide customers an increased level of safety during IV blood collection, convenience and to improve OSHA single-use holder compliance. Figure 1 shows a BD Vacutainer¿ Push Button Blood Collection Set with the needle protector removed prior to needle retraction.

## Reason for recall

Separation of front and rear barrels upon activation of the safety feature that retracts the needle

## Distribution

Worldwide distribution - US Nationwide distribution including the states of CT, FL, MO, TN, OH, TX, GA, NC, SC, IN, IL, PA, CO and countries of Trinidad and Tobago, Hong Kong.

## Key facts

- **Recall number:** Z-0193-2020
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-07-31
- **Report date:** 2019-10-30
- **Termination date:** 2020-07-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Franklin Lakes, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0193-2020

## Citation

> AI Analytics. FDA recall Z-0193-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0193-2020. Source: US FDA. Licensed CC0.

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