FDAJune 12, 2019device

BD Vacutainer LH (Lithium Heparin) 102 I.U. Plus Blood Collection Tubes, Catalog Number 368886

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

The hazard

False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.

What to do

FDA enforcement status: Terminated

Brands named

becton dickinsonbectonbecton dickinson

UPCs

30382903666646

Recall history

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

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BD Vacutainer LH (Lithium Heparin) 102 I.U. Plus Blood Collection Tubes, Catalog Number 368886 — Recall Details · AllClear