# FDA recall Z-3364-2018

> **B. Braun Medical, Inc.** · Class II · device recall initiated 2018-07-20.

## Product

CE18TB CONT EPIDURAL TRAY, Material Number 332222     Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

## Reason for recall

The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.

## Distribution

Worldwide Distribution: US (nationwide) and countries of:  Australia, Canada, Guatemala and Kuwait.

## Key facts

- **Recall number:** Z-3364-2018
- **Recalling firm:** B. Braun Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-07-20
- **Report date:** 2018-10-10
- **Termination date:** 2020-05-13

- **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-3364-2018

## Citation

> AI Analytics. FDA recall Z-3364-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-3364-2018. Source: US FDA. Licensed CC0.

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