# FDA recall Z-1436-2022

> **Becton Dickinson & Company** · Class II · device recall initiated 2022-05-09.

## Product

BD Connecta 3-Way Stopcocks  Catalog No. 394900 (OUS)

## Reason for recall

May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous material, under dosing/under infusion, contamination and/or air ingress.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of AK, AR, AZ, CA, CO, FL, GA, IL, IN, KS, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NV, NY, OH, OR, PA, SD, TN, TX, UT, VA, WA, WV and the countries of Belgium, China, India, Indonesia, Japan, Korea, Nepal, Philippines, Singapore, Sri Lanka, Thailand, Vietnam.

## Key facts

- **Recall number:** Z-1436-2022
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-05-09
- **Report date:** 2022-07-27

- **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-1436-2022

## Citation

> AI Analytics. FDA recall Z-1436-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1436-2022. Source: US FDA. Licensed CC0.

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