US Drug Recall Register
Class I · High risk Terminated Initiated Nov 8, 2019 (7 years ago)

UP2, Dietary Supplement, All Natural Libido for Men & Women, a) one pack, b) four pack…

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

Why it was recalled

Marketed without an Approved NDA/ANDA: Product contains undeclared sildenafil which was discovered through FDA analysis.

What was recalled

UP2, Dietary Supplement, All Natural Libido for Men & Women, a) one pack, b) four pack, c) ten pack capsules per carton, Exclusively Manufactured and Formulated by: Buy Wise Marketing, 4234 I-75 Business Spur, Sault Ste Marie, MI 49783, Ultimatepleasure2.com.

Recalling firm
Med Man Distribution, Inc.
Origin
Canada
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1036-2020

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.