# FDA recall Z-0318-2022

> **Magnolia Medical Technologies, Inc.** · Class II · device recall initiated 2021-11-02.

## Product

The Steripath Gen2 Blood Collection System    Model Number/Description  2700-21-EN	/ Steripath Gen2 Blood Collection System - 21G, Wide Neck  2700-23-EN	/ Steripath Gen2 Blood Collection System - 23G, Wide Neck  27BD-21-EN	/ Steripath Gen2 Blood Collection System - 21G, Long Neck  27BD-23-EN	/ Steripath Gen2 Blood Collection System - 23G, Long Neck

## Reason for recall

Due to an uptick of complaints associated with premature needle retraction of blood collection system.

## Distribution

U.S. Nationwide distribution in the states of MD, WV, DE, VA, DC, IN, MI, MA, SC, NY, IL, TX, AL, OK, GA, NE, FL, MO, CA, CO, NM, AR, WY, KS, PA, WA, MT, and AZ.

## Key facts

- **Recall number:** Z-0318-2022
- **Recalling firm:** Magnolia Medical Technologies, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-11-02
- **Report date:** 2021-12-08
- **Termination date:** 2023-05-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Seattle, WA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0318-2022

## Citation

> AI Analytics. FDA recall Z-0318-2022. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/Z-0318-2022. Source: US FDA. Licensed CC0.

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