Bard Peripheral Vascular Inc: Medical Device Recall in 2023 - (Recall #: Z-0027-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016

Product Classification:

Class II

Date Initiated: August 10, 2023

Date Posted: October 11, 2023

Recall Number: Z-0027-2024

Event ID: 92994

Reason for Recall:

Diameter mismatch between coaxial and biopsy needle (cutting cannula) in disposable core biopsy instrument kits, where the coaxial cannula inner diameter prohibits the biopsy needle (cutting cannula) from properly fitting into the coaxial cannula and accessing target tissue, which may lead to repeated procedure, and procedural complications, such as pain/discomfort, pneumothorax, and bleeding.

Status: Ongoing

Product Quantity: 1,545

Code Information:

UDI-DI: 00801741097393, Lot: 0001480774, Exp: 07/28/2025

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of PR, CO, TX, CA, WA, OR, AZ, NJ, NY, OH, NC, MD, MI, LA, IN, AK, TN and the countries of CA, AU, BE.

Voluntary or Mandated:

Voluntary: Firm initiated