---
title: "BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS) — FDA record Z-1435-2022 | Is It on Recall"
description: "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 biohazar"
url: https://isitonrecall.com/recall/fda-device-z-1435-2022-bd-connecta-stopcock-without-extension-tube-catalog-no-394605-ous/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS) — FDA record Z-1435-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 9, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS)
- **Reason**: 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.
- **Classification**: Class II
- **Recalling firm**: Becton Dickinson & Company
- **Quantity**: N/A
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1435-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1435-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | GTIN: 382903946051 Lot Numbers/Exp.Date: 1133181 4/30/2024 1117434 3/31/2024 1110835 3/31/2024 1119671 3/31/2024 1098353 3/31/2024 1098351 3/31/2024 1098350 3/31/2024 1110839 3/31/2024 1110842 3/31/2024 1067265 2/29/2024 1067268 2/29/2024 1067274 2/29/2024 1063372 2/29/2024 1067273 2/29/2024 1067264 2/29/2024 1034587 1/31/2024 1040899 1/31/2024 1034590 1/31/2024 1034594 1/31/2024 1040902 1/31/2024 1040891 1/31/2024 1034597 1/31/2024 1060806 2/29/2024 |

Match all identifying details in the current notice. A brand name alone is not enough.

## 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.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Jul 27, 2022
- **Recall initiation date**: May 9, 2022
- **Center classification date**: Jul 21, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1435-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Becton Dickinson & Company records](https://isitonrecall.com/brand/becton-dickinson-company/)
