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FDAApril 11, 2023device

Bard Mission Disposable Core Biopsy Instrument Kit: REF: 2010MSK, 20G x 10CM; REF: 2016MSK, 20G x 16CM

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

The hazard

Coaxial cannula internal diameter and length of biopsy instruments exceed the external diameter and length of the biopsy needle, prohibiting the biopsy needle from properly fitting into the coaxial cannula and accessing the target tissue, which could lead to procedure delay, and insufficient sample acquisition requiring a repeat procedure.

What to do

FDA enforcement status: Ongoing

Brands named

bard peripheral vascularbardbard peripheral

UPCs

0080174109708900801741097096

Recall history

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

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Bard Mission Disposable Core Biopsy Instrument Kit: REF: 2010MSK, 20G x 10CM; REF: 2016MSK, 20G x 16CM — Recall Details · AllClear