Bit & Bet Thumbs Up 7 Blue 69K, 10 capsules recall — FDA D-0388-2021
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of sildenafil and tadalafil.
Overview of recall records associated with Bit & Bet LLC, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of sildenafil and tadalafil.
This page summarizes recall records in which the official source identifies Bit & Bet LLC 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.