FDANovember 4, 2019device

Histoplasma Immunodiffusion (ID) Antigen; The IFU labeling is for multiple products which included Fungal Antigens, Positive Controls and ID Plates,and Immunodiffusion (ID) Plates for use in the ID Test, Histoplasma ID Antigen

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

The hazard

False positive results due to potential contamination of reagent.

What to do

FDA enforcement status: Terminated

Brands named

immuno mycologicsimmunoimmuno mycologics

UPCs

00816387020391

Recall history

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

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