The Recall Desk

FDA (Drugs) recall action 87653

Na Na Collection recalled 2 products on 2021-05-05

The FDA (Drugs) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2021-05-05
Critical
0
Units
—

Why these products were recalled

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

The agency’s own wording, quoted from the enforcement report.

1–2 of 2

  • SevereFDA (Drugs)··2021-05-05

    FDA Recalls PremierZen Platinum 5000 for Unapproved Active Ingredients

    Na Na Collection is recalling PremierZen Platinum 5000 capsules because FDA analysis detected unapproved active ingredients tadalafil and/or sildenafil.

    Product
    PremierZen Platinum 5000, Packaged in paper packaging with a pill blister, 1 capsule per box, Distributed by New Premier Group Los Angeles CA 90006
    Category
    Distribution
    0 states
  • SevereFDA (Drugs)··2021-05-05

    Triple SupremeZen Gold 3500 Recalled for Unapproved Active Ingredients

    Na Na Collection is recalling Triple SupremeZen Gold 3500 capsules because FDA analysis found unapproved active ingredients tadalafil and/or sildenafil.

    Product
    Triple SupremeZen Gold 3500, Packaged in paper packaging with a pill blister,1 capsule per box, Distributed by VIEW LIFE Distributors Los Angeles CA 90005 UPC 7 15122 05089 4
    Category
    Distribution
    0 states