Sildenafil and Tadalafil Recall: StuffbyNainax MR. 7 SUPER
Announced 2026-03-11 · FDA
FDA analysis found the product marketed without an approved NDA/ANDA contains undeclared sildenafil and tadalafil. The recall involves StuffbyNainax MR. 7 SUPER 700000 capsules that were distributed to four customers in the United States. The recall code covers all codes and the expiration date is 12/31/2029.
| Brand | StuffbyNainax |
|---|---|
| Product | 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 |
| Severity | critical |
| Units affected | 4 |
| Distribution | Product was distributed to 4 customers in the US. |
| Agency | FDA |
WHAT YOU SHOULD DO
- Stop using this product immediately.
- If you have any MR. 7 SUPER 700000 capsules, dispose of them or return them to the place of purchase per local guidelines.
- If you have used the product and have health concerns, consult a healthcare provider.
- Visit the FDA recall page for more information using recall number All codes and Exp 12/31/2029.
How to identify the recalled item
| Lot / date codes | All codes; Exp 12/31/2029 |
|---|---|
| Lot / date codes | All codes; Exp 12/31/2029 |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.