# FDA recall Z-2393-2021

> **Magnolia Medical Technologies, Inc.** · Class II · device recall initiated 2021-08-02.

## Product

Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This holder/adapter assembly may be used for the access of a specimen from Catheter Port to BD Vacutainer¿ Blood Collection or Urine Collection Tubes.

## Reason for recall

Product was shipped with the incorrect Transfer Adapter Instructions For Use (IFU).

## Distribution

U.S. Nationwide distribution i the states of AL, CO, FL, GA, IL, IN, MD, MI, NE, NY, PA, SC, TX, VA, WV, and WY.  O.U.S.: N/A

## Key facts

- **Recall number:** Z-2393-2021
- **Recalling firm:** Magnolia Medical Technologies, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-08-02
- **Report date:** 2021-09-08
- **Termination date:** 2023-02-22

- **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-2393-2021

## Citation

> AI Analytics. FDA recall Z-2393-2021. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-2393-2021. Source: US FDA. Licensed CC0.

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