US Drug Recall Register
Class I · High risk Terminated Initiated Aug 6, 2015 (11 years ago)

KABOOM action strips, Sexual Performance Strips, packaged in 6.4oz box 12 strips per box…

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

Why it was recalled

Marketed Without An Approved NDA/ANDA: presence of undeclared Sulfoaildenafil.

What was recalled

KABOOM action strips, Sexual Performance Strips, packaged in 6.4oz box 12 strips per box, Nutrology USA LLC

Recalling firm
Blue Square Market, Inc.
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0297-2016

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.