← FDA ENFORCEMENT
D-0397-2026Class I

StuffbyNainax

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
SPEQ quality domain
Documentation & Change Control
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
2026-07-22Class ID'Dioses Fruit Pops, Inc.2026-07-22Class IIFayus Inc.2026-07-22Class ID'Dioses Fruit Pops, Inc.2026-07-22Class ID'Dioses Fruit Pops, Inc.
See all Documentation & Change Control recalls →

Data: U.S. FDA openFDA enforcement API. 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.