Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bard Marquee Disposable Core Biopsy Instrument Kit Recalled by Bard Peripheral Vascular Inc Due to Diameter mismatch between coaxial and biopsy needle (cutting...
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 Instrument Kit, REF: MQK2016
Quantity: 1,545
Why Was This Recalled?
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.
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