FDAJuly 30, 2025drug

RECOMBINATE, [Antihemophilic Factor (Recombinant)], 5 mL vials, Rx Only, Takeda Pharmaceuticals USA, Cambridge, MA 02142, NDC: 00944-2843-01

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

The hazard

CGMP Deviations - Product was exposed to temperatures outside the product's labeled storage requirements.

What to do

FDA enforcement status: Ongoing

Brands named

cardinal healthcardinal

UPCs

00944284301

Recall history

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

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