FDA Recall D-1235-2014
Haute Health, LLC · Williamstown, NJ
Class I — life-threatening Terminated 489 days on record
Highest impact — Class I recall — FDA determination of strong likelihood of serious adverse health consequence or death.
Product
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.
Reason for recall
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.
Recall record
- Recall number
D-1235-2014- Classification
- Class I
- Status
- Terminated
- Voluntary or mandated
- Voluntary: Firm initiated
- Firm notification
- Press Release
- Distribution
- Nationwide and internationally via internet sales.
- Recall initiated
- 2013-09-27
- Classified by FDA Center
- 2014-04-15
- FDA published
- 2014-04-23
- Terminated
- 2015-01-29
- Recalling firm
- Haute Health, LLC
- Firm location
- Williamstown, NJ