FDA recall, , High risk
MR. 7 Super 700000 Capsules
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil.
Summary by Recall Canary from the FDA notice
What happened
StuffbyNainax of Huntsville, Texas recalled MR. 7 SUPER 700000 capsules, 1 capsule blister card, distributed by mR. 7, because FDA analysis revealed the presence of undeclared sildenafil and tadalafil. The product was distributed to 4 customers in the US.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
Compare the details below with your product and check the FDA notice to confirm whether it is affected.
MR. 7 Super 700000 capsules, 1 capsule blister card, Distributed by mR. 7
- Lot code
- All codes; Exp 12/31/2029
Recall details
- Company began the recall
- Sold in
Product was distributed to 4 customers in the US.
- Company
- StuffbyNainaxHuntsville, Texas
- Hazard
- Hidden drug ingredient
- Risk
High risk
There is a reasonable chance that taking it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- Event ID
- 98256
- Recall number
- D-0397-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report
In FDA's weekly enforcement report
Classified by FDA
Listed on Recall Canary
