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D-0397-2026Class I

StuffbyNainax

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
StuffbyNainax
Product type
Drug
Status
Ongoing
Report date
2026-03-11
Distribution
Product was distributed to 4 customers in the US.
Firm state
TX
Product quantity
4
Initiated by
Voluntary: Firm initiated
Reason for recall

Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil

Product description

MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7

Code / lot info

All codes; Exp 12/31/2029

Other recalls SPEQ maps to Documentation & Change Control
See all Documentation & Change Control recalls →

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →