Class I โ€” Serious Health Hazard

Serious health hazard โ€” there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

Titanium 4000 Recalled by D.B.P. Distribution Due to Undeclared Sildenafil

Date: April 23, 2019
Company: D.B.P. Distribution
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact D.B.P. Distribution directly.

Affected Products

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

Quantity: unknown

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About D.B.P. Distribution

D.B.P. Distribution has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report