# FDA recall Z-2427-2020

> **Argon Medical Devices, Inc** · Class II · device recall initiated 2019-12-02.

## Product

BioPince Full  Core Biopsy Instrument 16ga x 15cm.,Use with Optional CO-Axial Needle MCXS1615BP. QTY.: 5/CS - Product Usage: The disposable, automatic BioPince Full Core Biopsy Instrument is used to obtain multiple core samples from soft tissue such as liver, kidney, abdominal masses, etc.

## Reason for recall

Incorrect product labeling.

## Distribution

Worldwide distribution - US Nationwide including in the states of TX, IL, FL, KS, MD, CA, WA, NY, WI, PA and the countries of United Arab Emirates (Dubai), Spain, Canada.

## Key facts

- **Recall number:** Z-2427-2020
- **Recalling firm:** Argon Medical Devices, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-12-02
- **Report date:** 2020-07-01
- **Termination date:** 2022-11-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Athens, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2427-2020

## Citation

> AI Analytics. FDA recall Z-2427-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2427-2020. Source: US FDA. Licensed CC0.

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