FDAApril 23, 2019drug

Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000 UPC 86077000020

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

The hazard

Marketed without an approved NDA/ANDA: undeclared sildenafil and tadalafil.

What to do

FDA enforcement status: Terminated

Brands named

d b p distribution

UPCs

86077000020

Recall history

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

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