FDAFDA · Food and drugs·Recall number F-0215-2014
EDGE, Item number 21-620, dietary supplement, 60 packet per box. The Edge product includes two different packets of capsules - a "Before" packet and an "After" packet. The suggested use for the After packet is one packet (or 6 capsules) per day. The suggested use for the "Before" packet is one packet (or 4 capsules) per day.
Published November 27, 2013 · Recall initiated: October 23, 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
EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- New Algae Company
- Distributor
- Distributed nationwide.
- Lot
- Lot BO1 and AO1, Expiration date Aug 2015
- Risk classification
- Class I
- Area (FDA)
- food
- Country
- United States
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