US Drug Recall Register
Class I · High risk Terminated Initiated Apr 23, 2019 (7 years ago)

Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

What was recalled

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

Recalling firm
D.B.P. Distribution
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1292-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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