FDAFDA · Food and drugs·Recall number D-0083-2025
VitalityXtra Capsules, 500 mg, packaged in 10 count blisters in cartons, Distributed by: VitalityXtra, San Francisco, CA www.vitalityxtra.com
Published December 11, 2024 · Recall initiated: November 4, 2024
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 an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Boulla LLC
- Distributor
- Nationwide within the United States
- Lot
- Lot #: 230811, Exp: 08/11/2025
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.