# FDA recall Z-3144-2024

> **B. Braun Medical, Inc.** · Class II · device recall initiated 2024-08-08.

## Product

AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual Manifold, Four-way Stopcock, Model/Catalog Number: 472036

## Reason for recall

Potential for product leakage from the Spin Lock Connector on the distal end of the device due to the migration of excess solvent during the assembly process.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-3144-2024
- **Recalling firm:** B. Braun Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-08
- **Report date:** 2024-09-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Allentown, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3144-2024

## Citation

> AI Analytics. FDA recall Z-3144-2024. Retrieved 2026-07-10 from https://api.ai-analytics.org/recall/Z-3144-2024. Source: US FDA. Licensed CC0.

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