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.
Overview of recall records associated with Miracle 8989, including dates, categories and classifications where available.
Classification mix: Class I: 2.
Marketed without an approved NDA/ANDA - Product found to be tainted with Sildenafil and Tadalafil.
Marketed without an approved NDA/ANDA - Product found to be tainted with Sildenafil and Tadalafil.
This page summarizes recall records in which the official source identifies Miracle 8989 as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.