FDAJune 28, 2022device

BIOPHEN UFH Control Plasma

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

The hazard

Incorrect product labeling was included in the package.

What to do

FDA enforcement status: Terminated

Brands named

aniara diagnosticaaniara

UPCs

03663537008290

Recall history

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

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