FDAJuly 2, 2024device

BioPince Ultra Full Core Biopsy Instrument: REF: REF: 360-1080-01, 360-1080-02, 360-1080-03, 360-1580-01, 360-1580-02, 360-1580-03, 360-2080-01, 360-2080-02, 360-2080-03, 370-1080-01, 370-1080-02, 370-1080-03, 370-1580-01, 370-1580-02, 370-1580-03; Tru-Core II Biopsy Instrument, REF: 763114100x, ...

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

The hazard

Holes have been identified in biopsy instrument packaging trays compromising the sterile barrier, which may lead to cross contamination, or the introduction of micro-organisms into the access site, which could lead to an infectious process, bacteremia, or sepsis.

What to do

FDA enforcement status: Ongoing

Brands named

argon medical devicesargonargon medical

UPCs

208863330043730088633300437920886333224009008863332240052088633322401600886333224012208863330043590088633300435520886333224023008863332240292088633322403000886333224036

Recall history

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

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BioPince Ultra Full Core Biopsy Instrument: REF: REF: 360-1080-01, 360-1080-02, 360-1080-03, 360-1580-01, 360-1580-02, 360-1580-03, 360-2080-01, 360-2080-02, 360-2080-03, 370-1080-01, 370-1080-02, 370-1080-03, 370-1580-01, 370-1580-02, 370-1580-03; Tru-Core II Biopsy Instrument, REF: 763114100x, ... — Recall Details · AllClear