BARD MARQUEE Disposable Core Biopsy Instruments XX.Xcm, XX.Xcm, XXg x XXcm REF XXXXXXX Note -...
FDA Device Recall #Z-1289-2021 — Class II — January 14, 2021
Recall Summary
| Recall Number | Z-1289-2021 |
| Classification | Class II — Moderate risk |
| Date Initiated | January 14, 2021 |
| Status | Terminated |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Bard Peripheral Vascular Inc |
| Location | Tempe, AZ |
| Product Type | Devices |
| Quantity | Total 131,876 kits (102,210 kits U.S. and 29,666 kits O.U.S.) |
Product Description
BARD MARQUEE Disposable Core Biopsy Instruments XX.Xcm, XX.Xcm, XXg x XXcm REF XXXXXXX Note - for definition of the "X's refer to Tyvek Lid Label.pdf" uploaded in Associated Documents
Reason for Recall
Due to the Penetration Depth Switch used to select the desired penetration depth of the biopsy needle for soft tissue biopsies, detaches from the device during use.
Distribution Pattern
U.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, Puerto Rico, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY O.U.S.: Australia, Belgium, Canada, Europe, India, and Singapore
Lot / Code Information
Catalog and Product Description MQ1210 BARD MARQUEE Disposable Core Biopsy Instrument, 12g x 10cm, MQ1213 BARD MARQUEE Disposable Core Biopsy Instrument, 12g x 13cm, MQ1410 BARD MARQUEE Disposable Core Biopsy Instrument, 14g x 10cm, MQ1413 BARD MARQUEE Disposable Core Biopsy Instrument, 14g x 13cm, MQ1416 BARD MARQUEE Disposable Core Biopsy Instrument, 14g x 16cm, MQ1610 BARD MARQUEE Disposable Core Biopsy Instrument, 16g x 10cm, MQ1616 BARD MARQUEE Disposable Core Biopsy Instrument, 16g x 16cm, MQ1620 BARD MARQUEE Disposable Core Biopsy Instrument, 16g x 20cm, MQ1810 BARD MARQUEE Disposable Core Biopsy Instrument, 18g x 10cm, MQ1816 BARD MARQUEE Disposable Core Biopsy Instrument, 18g x 16cm, MQ1820 BARD MARQUEE Disposable Core Biopsy Instrument, 18g x 20cm, MQ1825 BARD MARQUEE Disposable Core Biopsy Instrument, 18g x 25cm, MQK1210 BARD MARQUEE Disposable Core Biopsy Instrument Kit, 12g x 10cm, MQK1213 BARD MARQUEE Disposable Core Biopsy Instrument Kit, 12g x 13cm, MQK1410 BARD MARQUEE Disposable Core Biopsy Instrument Kit, 14g x 10cm, MQK1413 BARD MARQUEE Disposable Core Biopsy Instrument Kit, 14g x 13cm, MQK1416 BARD MARQUEE Disposable Core Biopsy Instrument Kit, 14g x 16cm, MQK1610 BARD MARQUEE Disposable Core Biopsy Instrument Kit, 16g x 10cm, MQK1810 BARD MARQUEE Disposable Core Biopsy Instrument Kit, 18g x 10cm, MQK1816 BARD MARQUEE Disposable Core Biopsy Instrument Kit, 18g x 16cm, MQK1820 BARD MARQUEE Disposable Core Biopsy Instrument Kit, 18g x 20cm, MQK1825 BARD MARQUEE Disposable Core Biopsy Instrument Kit, 18g x 25cm, MQK2010 BARD MARQUEE Disposable Core Biopsy Instrument Kit, 20g x 10cm, MQK2016 BARD MARQUEE Disposable Core Biopsy Instrument Kit, 20g x 16cm UDI Codes: (01)801741097119(17)230328(10)0001353340, (01)801741097119(17)230328(10)0001353342, (01)801741097119(17)230328(10)0001353401, (01)801741097119(17)230328(10)0001356645, (01)801741097119(17)230328(10)0001358065, (01)801741097119(17)230428(10)0001359983, (01)801741097119(17)230628(10)0001369253, (01)801741097126(17)230328(10)0001353402, (01)801741097126(17)230428(10)0001359984, (01)801741097126(17)230628(10)0001369256, (01)801741097133(17)230328(10)0001353403, (01)801741097133(17)230328(10)0001353404, (01)801741097133(17)230328(10)0001356410, (01)801741097133(17)230328(10)0001356409, (01)801741097133(17)230328(10)0001356886, (01)801741097133(17)230328(10)0001356888, (01)801741097133(17)230428(10)0001359150, (01)801741097133(17)230428(10)0001359152, (01)801741097133(17)230428(10)0001359149, (01)801741097133(17)230428(10)0001359151, (01)801741097133(17)230428(10)0001359988, (01)801741097133(17)230528(10)0001363603, (01)801741097133(17)230528(10)0001363604, (01)801741097133(17)230528(10)0001364078, (01)801741097133(17)230528(10)0001364076, (01)801741097133(17)230528(10)0001364077, (01)801741097133(17)230528(10)0001368474, (01)801741097133(17)230628(10)0001369045, (01)801741097133(17)230628(10)0001369046, (01)801741097140(17)230328(10)0001357081, (01)801741097140(17)230628(10)0001369273, (01)801741097157(17)230328(10)0001357079, (01)801741097164(17)230328(10)0001353246, (01)801741097164(17)230328(10)0001356414, (01)801741097164(17)230428(10)0001359989, (01)801741097164(17)230528(10)0001364079, (01)801741097164(17)230628(10)0001369264, (01)801741097171(17)230328(10)0001356999, (01)801741097171(17)230428(10)0001359990, (01)801741097188(17)230328(10)0001353723, (01)801741097195(17)230328(10)0001353492, (01)801741097195(17)230428(10)0001359991, (01)801741097195(17)230528(10)0001364091, (01)801741097195(17)230628(10)0001369267, (01)801741097201(17)230328(10)0001353722, (01)801741097218(17)230528(10)0001364092, (01)801741097218(17)230528(10)0001364093, (01)801741097218(17)230628(10)0001369270, (01)801741097225(17)230328(10)0001353721, (01)801741097225(17)230328(10)0001355807, (01)801741097225(17)230428(10)0001359994, (01)801741097225(17)230528(10)0001364090, (01)801741097263(17)230328(10)0001353400, (01)801741097263(17)230328(10)0001353399, (01)801741097263(17)230328(10)0001356646, (01)801741097263(17)230428(10)0001359178, (01)801741097263(17)230528(10)0001364069, (01)801741097263(17)230528(10)0001364070, (01)801741097263(17)230528(10)0001366667, (01)801741097263(17)230628(10)0001369252, (01)801741097263(17)230628(10)0001371860, (01)801741097270(17)230528(10)0001364072, (01)801741097270(17)230628(10)0001369259, (01)801741097287(17)230328(10)0001353727, (01)801741097287(17)230328(10)0001356411, (01)801741097287(17)230328(10)0001356412, (01)801741097287(17)230428(10)0001358408, (01)801741097287(17)230428(10)0001358409, (01)801741097287(17)230428(10)0001358414, (01)801741097287(17)230428(10)0001359999, (01)801741097287(17)230428(10)0001358413, (01)801741097287(17)230528(10)0001364084, (01)801741097287(17)230528(10)0001364085, (01)801741097287(17)230528(10)0001364082, (01)801741097287(17)230528(10)0001364080, (01)801741097287(17)230528(10)0001364081, (01)801741097287(17)230528(10)0001367194, (01)801741097287(17)230528(10)0001367195, (01)801741097287(17)230528(10)0001367196, (01)801741097287(17)230528(10)0001368556, (01)801741097287(17)230528(10)0001368555, (01)801741097287(17)230528(10)0001368760, (01)801741097287(17)230628(10)0001369292, (01)801741097294(17)230428(10)0001360001, (01)801741097300(17)230228(10)0001347094, (01)801741097300(17)230328(10)0001357065, (01)801741097317(17)230328(10)0001357859, (01)801741097317(17)230528(10)0001364088, (01)801741097317(17)230628(10)0001369278, (01)801741097348(17)230328(10)0001353725, (01)801741097348(17)230428(10)0001360028, (01)801741097348(17)230628(10)0001369289, (01)801741097355(17)230528(10)0001364089, (01)801741097355(17)230628(10)0001369284, (01)801741097362(17)230628(10)0001369290, (01)801741097379(17)230328(10)0001353724, (01)801741097379(17)230428(10)0001360029, (01)801741097386(17)230628(10)0001369272, (01)801741097393(17)230428(10)0001360030, (01)801741097393(17)230628(10)0001369276, Lot Numbers: 0001353340, 0001353342, 0001353401, 0001356645, 0001358065, 0001359983, 0001369253, 0001353402, 0001359984, 0001369256, 0001353403, 0001353404, 0001356410, 0001356409, 0001356886, 0001356888, 0001359150, 0001359152, 0001359149, 0001359151, 0001359988, 0001363603, 0001363604, 0001364078, 0001364076, 0001364077, 0001368474, 0001369045, 0001369046, 0001357081, 0001369273, 0001357079, 0001353246, 0001356414, 0001359989, 0001364079, 0001369264, 0001356999, 0001359990, 0001353723, 0001353492, 0001359991, 0001364091, 0001369267, 0001353722, 0001364092, 0001364093, 0001369270, 0001353721, 0001355807, 0001359994, 0001364090, 0001353400, 0001353399, 0001356646, 0001359178, 0001364069, 0001364070, 0001366667, 0001369252, 0001371860, 0001364072, 0001369259, 0001353727, 0001356411, 0001356412, 0001358408, 0001358409, 0001358414, 0001359999, 0001358413, 0001364084, 0001364085, 0001364082, 0001364080, 0001364081, 0001367194, 0001367195, 0001367196, 0001368556, 0001368555, 0001368760, 0001369292, 0001360001, 0001347094, 0001357065, 0001357859, 0001364088, 0001369278, 0001353725, 0001360028, 0001369289, 0001364089, 0001369284, 0001369290, 0001353724, 0001360029, 0001369272, 0001360030, 0001369276
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|---|---|---|---|
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| Z-1244-2025 | Class I | Rotarex Atherectomy System and Instructions for... | Feb 5, 2025 |
| Z-0467-2025 | Class II | Bard Marquee Disposable Core Biopsy Instrument ... | Sep 30, 2024 |
Frequently Asked Questions
Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.
Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.
Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.
What Should You Do?
Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.