FDA recall record

Miracle 8989 PremierZEN Platinum 8000 capsule, 1-count blister card (UPC 7 28175 42185 6) recall — FDA D-0634-2021

Marketed without an approved NDA/ANDA - Product found to be tainted with Sildenafil and Tadalafil.

Class Iclassification
D-0634-2021official record ID
Jun 30, 2021report date

Recall record at a glance

Official recordD-0634-2021
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmMiracle 8989
Report dateJun 30, 2021
Recall initiation dateMay 18, 2021
QuantityUnknown
LocationDallas, TX, United States

Official product description

PremierZEN Platinum 8000 capsule, 1-count blister card (UPC 7 28175 42185 6), packaged in 12 cards per box (UPC 7 28175 42183 2), Distributed by: New Premier Group, Los Angeles, CA 90006

Why the product was recalled

Marketed without an approved NDA/ANDA - Product found to be tainted with Sildenafil and Tadalafil.

Distribution information

USA Nationwide

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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