Critical Alert
StuffbyNainax Recalls MR
This is a Class I recall — the most serious type. There is a reasonable probability of serious health consequences or death.
Source: FDA
CriticalRecall #D-0397-2026Drug / Pharmaceutical
StuffbyNainax Recalls MR
StuffbyNainax · Class I — Most Serious
Product Description
MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7
Reason for Recall
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil
FDA Classification
Class I — Most Serious
A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Distribution
Product was distributed to 4 customers in the US.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
The FDA has classified this as a Class I recall — the most serious classification reserved for situations where there is a reasonable probability that use of, or exposure to, the product will cause serious adverse health consequences or death. StuffbyNainax initiated this recall of pharmaceutical product on December 15, 2025 affecting 4. Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil. The product was distributed nationwide. Consumers who have this product should stop using it immediately and contact the recalling firm.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medical Product Contamination.