QMart: Drug Recall
Recall #D-0369-2021 · 03/31/2021
Class II: Risk
Recall Details
- Recall Number
- D-0369-2021
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- QMart
- Status
- Ongoing
- Date Initiated
- 03/31/2021
- Location
- Elmwood Park, NJ, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 500 boxes
Reason for Recall
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.
Product Description
PremierZen Extreme 3000, Male Sexual Performance Enhancement, 1 Capsule, UPC 728175421887
Distribution Pattern
USA Nationwide
Other Recalls by QMart
- Class II: Risk 03/31/2021
- Class II: Risk 03/31/2021
- Class II: Risk 03/31/2021
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.