FDA Drugs recall ·
MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7 recall
This is an FDA Class I recall — the most serious type.
- Recall number
- D-0397-2026
- Date
- (initiated December 15, 2025)
- Company / brand
- StuffbyNainax
2830 Lake Rd Apt 1102, Huntsville, TX, United States - Category
- Drugs › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 4
- Hazard tags
- Undeclared allergen
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7
Why was it recalled?
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
All codes; Exp 12/31/2029
Distribution
Product was distributed to 4 customers in the US.
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (drugs), recall D-0397-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.