# FDA recall Z-2111-2018

> **CareFusion 303, Inc.** · Class II · device recall initiated 2017-11-06.

## Product

Alaris Extension Sets with microbore tubing Model 20022 and 30914     Is used to administer fluid and medications from a syringe to the patient through a needle or catheter inserted into the patient's artery or vein. These model codes are extension sets that can be used with IV administration sets. The set s components are commonly found on intravascular administration sets and extension sets. It includes a microbore tubing, a slide clamp, male and female luer.

## Reason for recall

Reports of incorrect priming volume due to manufacturing with incorrect tubing.

## Distribution

US Distribution to states of:  CA, IL, IN, KS, NE, NJ, TX, UT, VA and WA

## Key facts

- **Recall number:** Z-2111-2018
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-11-06
- **Report date:** 2018-06-13
- **Termination date:** 2020-12-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Diego, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2111-2018

## Citation

> AI Analytics. FDA recall Z-2111-2018. Retrieved 2026-07-11 from https://api.ai-analytics.org/recall/Z-2111-2018. Source: US FDA. Licensed CC0.

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