Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BARD MARQUEE Disposable Core Biopsy Instruments XX.Xcm Recalled by Bard Peripheral Vascular Inc Due to Due to the Penetration Depth Switch used to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Bard Peripheral Vascular Inc directly.
Affected Products
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
Quantity: Total 131,876 kits (102,210 kits U.S. and 29,666 kits O.U.S.)
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bard Peripheral Vascular Inc
Bard Peripheral Vascular Inc has 136 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report