PlainRecalls
FDA Drug Critical Class I Terminated

BLACK LABEL X capsules, 60-count bottles, Manufactured for: Making it A Lifestyle, L.L.C.

Reported: December 28, 2016 Initiated: April 29, 2016 #D-0220-2017

Product Description

BLACK LABEL X capsules, 60-count bottles, Manufactured for: Making it A Lifestyle, L.L.C.

Reason for Recall

Marketed without an approved NDA/ANDA - presence of undeclared sildenafil.

Details

Recalling Firm
Making It a Lifestyle
Units Affected
1000 bottles
Distribution
Nationwide
Location
Corpus Christi, TX

Frequently Asked Questions

What product was recalled?
BLACK LABEL X capsules, 60-count bottles, Manufactured for: Making it A Lifestyle, L.L.C.. Recalled by Making It a Lifestyle. Units affected: 1000 bottles.
Why was this product recalled?
Marketed without an approved NDA/ANDA - presence of undeclared sildenafil.
Which agency issued this recall?
This recall was issued by the FDA Drug on December 28, 2016. Severity: Critical. Recall number: D-0220-2017.