Argon Medical Devices, Inc: Medical Device Recall in 2020 - (Recall #: Z-2427-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: December 2, 2019

Date Posted: July 1, 2020

Recall Number: Z-2427-2020

Event ID: 85426

Reason for Recall:

Incorrect product labeling.

Status: Terminated

Product Quantity: 165 units in U.S. and 330 units Internationally

Code Information:

Lot No.: 11277175; Model # 370-1580-01, 16ga x 15cm, for use with Optional Co-axial Needle MCXS1615BP

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated