FDAFDA · Food and drugs·Recall number D-0383-2021
Triple SupremeZen Plus 3500, packaged in cardboard blisters containing one capsule per card, Distributed by Yolo Studio, Cliffside Park, NJ
Published May 26, 2021 · Recall initiated: April 6, 2021
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Hyobin LLC
- Distributor
- USA Nationwide
- Lot
- all lots
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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