Class I · Most seriousActive recall
MR. 7 SUPER 700000 capsules
A reasonable chance it could cause serious harm or death.
Does this affect you?
Check your lot numberAll codes; Exp 12/31/2029
Where it was soldProduct was distributed to 4 customers in the US.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | mR. 7 |
Show the full FDA record
| Full product label | MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7 |
| Recalling firm | StuffbyNainax |
| Distribution | Product was distributed to 4 customers in the US. |
| Quantity | 4 |
| Recall initiated | 2025-12-15 |
| Report date | 2026-03-11 |
| Recall completed | — |
| Recall number | D-0397-2026 |
| Classification | Class I |
| FDA status | Ongoing |
| Origin on file | Huntsville TX United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.