# FDA recall Z-2343-2018

> **B. Braun Medical, Inc.** · Class II · device recall initiated 2018-06-04.

## Product

26-Lead Transfer Set for use with APEX¿ Compounding System, Product Catalog Number 2112550

## Reason for recall

There is a potential for valves on the 26-Lead Transfer Set to be incorrectly oriented.   When a transfer set with an incorrectly oriented valve is installed on the system, there is potential for unintended admixture.

## Distribution

The products were distributed to the following US states:  AL, CA, CO, CT, FL, GA, IL, LA, MA, MD, MI, MN, MO, NC, NJ, NV, OH, PA, TX, and WA.

## Key facts

- **Recall number:** Z-2343-2018
- **Recalling firm:** B. Braun Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-06-04
- **Report date:** 2018-07-11
- **Termination date:** 2020-01-13

- **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-2343-2018

## Citation

> AI Analytics. FDA recall Z-2343-2018. Retrieved 2026-06-15 from https://api.ai-analytics.org/recall/Z-2343-2018. Source: US FDA. Licensed CC0.

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