MR. 7 SUPER 700000 capsules recall (StuffbyNainax)
DrugClass IOngoing
Summary: StuffbyNainax is recalling MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7. Reason: Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil.
What is being recalled
MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7
Why
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil
How serious is it
Class I is the most serious level: FDA considers there is a reasonable probability that using or being exposed to this product will cause serious health problems or death.
Where it was sold
Product was distributed to 4 customers in the US.
How to tell if yours is affected
All codes; Exp 12/31/2029
What to do
Check the product name, lot number and expiration date on your package against the codes above. If they match, do not stop taking a prescription medicine without talking to your doctor or pharmacist first; ask them about a replacement. Return or dispose of the product as your pharmacy advises.
Recall facts
| Recall number | D-0397-2026 |
| Category | Drug |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class I |
| Status | Ongoing |
| Recall started | December 15, 2025 |
| Reported | March 11, 2026 |
| Company | StuffbyNainax |
| Company location | Huntsville, TX, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 4 |
More recalls from StuffbyNainax · all drug recalls · recalls from December 2025