FDAJanuary 14, 2021device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

bard peripheral vascularbardbard peripheral

UPCs

801741097119801741097126801741097133801741097140801741097157801741097164801741097171801741097188801741097195801741097201801741097218801741097225

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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