MR. 7 SUPER 700000 capsules recalled for undeclared sildenafil
MR. 7 SUPER 700000 capsules contain hidden prescription drugs—sildenafil and tadalafil—that are not listed on the label. These are serious medications that can interact with other drugs and cause health problems. The product was sold without FDA approval.
From the FDA notice · Read the official notice ↗
What to do
- Stop using MR. 7 SUPER 700000 capsules immediately
- Do not take any remaining capsules from your blister card
- Consult your doctor or pharmacist if you have taken this product
- Report any adverse effects to the FDA at 1-888-SAFEFOOD or online at www.fda.gov/medwatch
Is yours affected?
Compare your label or packaging with the recalled product.
- Product
- MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7
- Sold in
- Nationwide
- Made for
- Adults
Details
- Units affected
- 4
- Illnesses reported
- None reported
- Manufactured in
- 2830 Lake Rd Apt 1102, N/A, Huntsville, TX, United States
- Classification
- Class I
- Recall number
- D-0397-2026
In the FDA's words
- Description
- MR. 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 All codes; Exp 12/31/2029 Distribution: Product was distributed to 4 customers in the US. Affected quantity: 4
- Hazard
- Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil