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Stuffbynainax

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Class I

  • The FDA’s most serious category — a reasonable probability of serious harm or death.
  • Refunds don't require a receipt, and you don't need proof of purchase.
  • FDA status: Ongoing.

What was recalled

Source: FDA · synced 29 Jul 2026 13:14
Check with your pharmacist Filed 2026-03-11

Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil

MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7

Check these codes: All codes; Exp 12/31/2029

4 · distributed product was distributed to 4 customers in the us. Recall D-0397-2026 on FDA.gov ↗
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