Recall RadarMR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil
Read the official FDA notice →What to do
Stop using the product and check it against the description above. This recall is in the most serious category, meaning the agency believes it can cause serious injury or death — don't finish the package or use up what's left. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.
Details
- Recalling company
- StuffbyNainax — Huntsville, TX
- Severity
- Class I — serious
- Reported
- March 11, 2026
- Quantity
- 4
- Recall number
- D-0397-2026
- Status
- Ongoing
- Source
- FDA
Where it went
Product was distributed to 4 customers in the US.
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