# FDA recall Z-1426-2018

> **Carefusion 2200 Inc** · Class II · device recall initiated 2017-02-23.

## Product

Thoracentesis/ Paracentesis Kit 10/CS; STERILE;

## Reason for recall

The integrity of the sterile packaging is potentially compromised.

## Distribution

Nationwide, Australia, Brazil, Canada, China, Japan, Kuwait, Malaysia, Mexico, Netherlands, New Zealand, Philippines, Singapore, South Africa, Taiwan, Thailand, United Arab Emirates, Vietnam

## Key facts

- **Recall number:** Z-1426-2018
- **Recalling firm:** Carefusion 2200 Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-02-23
- **Report date:** 2018-04-25
- **Termination date:** 2019-07-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Vernon Hills, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1426-2018

## Citation

> AI Analytics. FDA recall Z-1426-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1426-2018. Source: US FDA. Licensed CC0.

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