FDAFDA · Food and drugs·Recall number D-1235-2014
Prolifta Dietary Supplement Prolifta, 400mg/capsule, Packaged in 1 and 2 capsule blister packs and 4, 12, and 24 capsule bottles Made in the USA Distributed by: Prolifta LLC 1+877.239.8231 www.proliftaherbal.com.
Published April 23, 2014 · Recall initiated: September 27, 2013
Status when published: Terminated — 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: Dietary supplement may contain amounts of an active ingredient found in some FDA-approved drugs for erectile dysfunction (ED) making the dietary supplement an unapproved drug.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Haute Health, LLC
- Distributor
- Nationwide and internationally via internet sales.
- Lot
- All lot codes and expiration dates.
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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