---
title: "Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016 — FDA record Z-0027-2024 | Is It on Recall"
description: "Diameter mismatch between coaxial and biopsy needle (cutting cannula) in disposable core biopsy instrument kits, where the coaxial cannula inner diameter prohib"
url: https://isitonrecall.com/recall/fda-device-z-0027-2024-bard-marquee-disposable-core-biopsy-instrument-kit-ref-mqk2016/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016 — FDA record Z-0027-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Aug 10, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016
- **Reason**: 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.
- **Classification**: Class II
- **Recalling firm**: Bard Peripheral Vascular Inc
- **Quantity**: 1,545
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0027-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0027-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI-DI: 00801741097393, Lot: 0001480774, Exp: 07/28/2025 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Oct 11, 2023
- **Recall initiation date**: Aug 10, 2023
- **Center classification date**: Oct 4, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0027-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Bard Peripheral Vascular Inc records](https://isitonrecall.com/brand/bard-peripheral-vascular-inc/)
