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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

Bard Marquee Biopsy Instruments Recalled for Needle Detachment Risk

Agency Publication Date: November 15, 2024
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Summary

Approximately 71,498 Bard Marquee Disposable Core Biopsy Instrument Kits are being recalled because the needles may not be properly secured inside the device. This is due to a manufacturing defect where a retention notch is missing, which could cause the needle to detach or become misplaced during medical procedures. While no injuries or incidents have been reported to date, this defect could cause serious complications during use.

Risk

If the needle detaches from the instrument, it can be misplaced within a patient's body, which could result in internal tissue damage and bleeding.

What You Should Do

  1. This recall affects Bard Marquee Disposable Core Biopsy Instrument Kits and individual instruments, including models MQK1210, MQ1210, MQK1213, and MQ1213.
  2. To determine if your product is affected, check the model (REF) number and the lot number/expiration date printed on the product label or packaging. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.
  4. For additional questions, call the FDA at 1-888-463-6332 (1-888-INFO-FDA).

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Bard Marquee Disposable Core Biopsy Instrument Kit (12G X 10 CM)
Variants: 12G X 10 CM
Model / REF:
MQK1210
Lot Numbers:
1490758 (Exp 9/28/2025)
1506044 (Exp 1/28/2026)
1506045 (Exp 1/28/2026)
1511827 (Exp 2/28/2026)
1514692 (Exp 3/28/2026)
1518977 (Exp 4/28/2026)
1518978 (Exp 4/28/2026)
1518979 (Exp 4/28/2026)
1519143 (Exp 4/28/2026)
1520507 (Exp 5/28/2026)
1520508 (Exp 5/28/2026)
1522157 (Exp 5/28/2026)
1522158 (Exp 5/28/2026)
1522577 (Exp 5/28/2026)
1523785 (Exp 6/28/2026)
1523914 (Exp 6/28/2026)
1523915 (Exp 6/28/2026)
1525370 (Exp 6/28/2026)
1525371 (Exp 6/28/2026)
1525373 (Exp 6/28/2026)
1528417 (Exp 7/28/2026)
1528418 (Exp 7/28/2026)
1528495 (Exp 7/28/2026)
1528496 (Exp 7/28/2026)
1528497 (Exp 7/28/2026)
1528560 (Exp 7/28/2026)
0001618867 (Exp 3/28/2028)
0001620281 (Exp 3/28/2028)
0001632675 (Exp 6/28/2028)
UDI:
00801741097263
Product: Bard Marquee Disposable Core Biopsy Instrument (12G X 10 CM)
Variants: 12G X 10 CM
Model / REF:
MQ1210
Lot Numbers:
1514460 (Exp 3/28/2026)
1514461 (Exp 3/28/2026)
1519144 (Exp 4/28/2026)
1519145 (Exp 4/28/2026)
1519456 (Exp 4/28/2026)
1520066 (Exp 5/28/2026)
1520067 (Exp 5/28/2026)
1520506 (Exp 5/28/2026)
1523783 (Exp 6/28/2026)
1523784 (Exp 6/28/2026)
0001618258 (Exp 3/28/2028)
0001631611 (Exp 6/28/2028)
0001633216 (Exp 7/28/2028)
UDI:
00801741097119
Product: Bard Marquee Disposable Core Biopsy Instrument Kit (12G X 13 CM)
Variants: 12G X 13 CM
Model / REF:
MQK1213
Lot Numbers:
1543517 (Exp 10/28/2026)
1559312 (Exp 2/28/2027)
1562724 (Exp 3/28/2027)
1569737 (Exp 4/28/2027)
1581652 (Exp 7/28/2027)
UDI:
00801741097270
Product: Bard Marquee Disposable Core Biopsy Instrument (12G X 13 CM)
Variants: 12G X 13 CM
Model / REF:
MQ1213
Lot Numbers:
1558191 (Exp 2/28/2027)
1559313 (Exp 2/28/2027)
UDI:
00801741097126

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95491
Status: Active
Manufacturer: Bard Peripheral Vascular Inc
Sold By: Authorized Medical Distributors; Hospitals; Surgical Centers
Manufactured In: United States
Units Affected: 71,498
Distributed To: Washington, Louisiana, Minnesota, Pennsylvania, Utah, South Carolina, Oklahoma, Kentucky, Arizona, Illinois, Texas, New Jersey, New York, Florida, Tennessee, Indiana, Ohio, North Carolina, Colorado, Virginia, Georgia, Maryland, California, Alabama, Wisconsin, Missouri, Iowa, Connecticut, Nebraska, Michigan, Mississippi, Nevada, Kansas, Oregon, South Dakota, Idaho, New Hampshire, Rhode Island, Wyoming, Arkansas, Massachusetts, Delaware, North Dakota, New Mexico, Alaska, Puerto Rico
Agency Last Updated: January 28, 2026

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.