Class I
Drug Recall: MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7
StuffbyNainax · December 15, 2025
Reason for Recall
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil
Distribution
Product was distributed to 4 customers in the US.
States Affected
IN
Quantity Affected
4
Source: FDA (openFDA Drug Enforcement)
Recall number: D-0397-2026
Status: ongoing
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