# FDA recall Z-3030-2017

> **CareFusion 303, Inc.** · Class II · device recall initiated 2017-06-30.

## Product

VersaSafe Plastic Cannula - 11 Gauge, Model 9391-0200    Product Usage:  Used with secondary IV sets or syringes with a female luer lock adapter to administer fluid and medications through a needle or catheter inserted into a patients artery or vein.

## Reason for recall

Punctures in blister packaging that was detected during the packaging process.

## Distribution

Worldwide Distribution in the states of : CO, IL, IN, MD, MI, NY, OH, & TX. and foreign  countries of: Australia, New Zealand, & Japan.

## Key facts

- **Recall number:** Z-3030-2017
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-30
- **Report date:** 2017-08-23
- **Termination date:** 2021-02-03

- **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-3030-2017

## Citation

> AI Analytics. FDA recall Z-3030-2017. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-3030-2017. Source: US FDA. Licensed CC0.

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