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FDAJanuary 18, 2017device

BONE MARROW ASPIRATION NEEDLE 15G x 2.688 MAX and 15G x 4 MAX Intended for the purpose of harvesting bone and/or bone marrow specimens

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

The hazard

The recalling firm received a complaint from one of their customers of a potential defect in the forming of the primary package of the blister that may compromise the sterility of the product inside the tray.

What to do

FDA enforcement status: Terminated

Brands named

argon medical devicesargonargon medical

Recall history

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

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