FDA analysis shows StuffbyNainax's MR 7 SUPER 700000 capsules contain undeclared sildenafil and tadalafil. Consumers should stop using these capsules immediately as they were marketed without FDA approval.
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil
StuffbyNainax is recalling its MR 7 SUPER 700000 capsules because FDA testing found undeclared sildenafil and tadalafil. This means the product was sold without proper FDA approval, which could pose health risks.
The capsules were marketed without FDA approval and contain undeclared sildenafil (an erectile dysfunction drug) and tadalafil (a drug for erectile dysfunction and pulmonary hypertension). These substances can cause serious health issues, especially in people with heart conditions or those on other medications.
Anyone who owns or uses the MR 7 SUPER 700000 capsules. People with cardiovascular conditions or those taking other medications are at higher risk due to the undeclared drugs.
Check for the product name 'MR 7 SUPER 700000 capsules' with a 1-capsule blister card. The capsules were distributed by mR. 7 and expire on 12/31/2029.
Immediately stop using the MR 7 SUPER 700000 capsules as they contain undeclared sildenafil and tadalafil.
FDA analysis revealed the presence of undeclared sildenafil and tadalafil, meaning the product was marketed without FDA approval.
The undeclared sildenafil and tadalafil can cause serious health issues, especially for people with heart conditions or those taking other medications.
Look for the product name 'MR 7 SUPER 700000 capsules' with a 1-capsule blister card. The capsules were distributed by mR. 7 and expire on 12/31/2029.
We’ve drafted a message you can send StuffbyNainax to request your refund or repair — edit it as you like.
Subject: Recall D-0397-2026 — StuffbyNainax StuffbyNainax Hello, I own a StuffbyNainax that is covered by recall D-0397-2026 from StuffbyNainax. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
