# FDA recall Z-0467-2025

> **Bard Peripheral Vascular Inc** · Class II · device recall initiated 2024-09-30.

## Product

Bard Marquee Disposable Core Biopsy Instrument Kit:  BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210;  BARD MARQUEE 12G X 10 CM, REF: MQ1210;  BARD MARQUEE Kit 12G X 13 CM, REF: MQK1213;  BARD MARQUEE 12G X 13 CM, REF: MQ1213

## Reason for recall

Disposable biopsy instruments were potentially manufactured missing the backend notch retention feature on the needle that results in inadequate securing of the needle inside the device, which could lead to needle detachment and misplacement, which could lead to tissue damage and bleeding.

## Distribution

Worldwide - US Nationwide including in the states of WA, LA, MN, PA, UT, SC, OK, KY, AZ, IL, TX, NJ, NY, FL, TN, IN, OH, NC, CO, VA, GA, MD, CA, AL, WI, MO, IA, CT, NE, MI, MS, NV, KS, OR, SD, ID, NH, RI, WY, AR, MA, DE, ND, NM, AK, PR and the countries of Portugal, Spain, South Africa, Greece, United Arab Emirates, United Kingdom, Sweden, Finland, Belgium, Korea, Australia, Canada.

## Key facts

- **Recall number:** Z-0467-2025
- **Recalling firm:** Bard Peripheral Vascular Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-09-30
- **Report date:** 2024-11-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tempe, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0467-2025

## Citation

> AI Analytics. FDA recall Z-0467-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0467-2025. Source: US FDA. Licensed CC0.

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