D.B.P. Distribution recalls Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000 UPC 860770
Recalled May 22, 2019 · FDA recall D-1292-2019 · D.B.P. Distribution
Hazard
Marketed without an approved NDA/ANDA: undeclared sildenafil and tadalafil. · FDA Class I
Units
unknown
Sold at
Nationwide.
Description
Marketed without an approved NDA/ANDA: undeclared sildenafil and tadalafil.
Product
Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000 UPC 86077000020
Manufacturer(s)
D.B.P. Distribution
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →