EDGE, Item number 21-620, dietary supplement, 60 packet per box. The Edge product includes two different pa

Recall map → All recalls → 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. New Algae Company · reported 2013-11-27

Terminated This recall has been closed out by the agency.

Reason for recall: EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.
Classification: Class I
Recall initiated: 2013-10-23
Reported by the agency: 2013-11-27
Closed out (terminated): 2014-03-05
Recalling firm: New Algae Company
Klamath Falls, OR
United States
This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.
Distribution (the agency's own words): Distributed nationwide.
States we parsed from that text: AK AL AR AZ CA CO CT DC DE FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO MS MT NC ND NE NH NJ NM NV NY OH OK OR PA RI SC SD TN TX UT VA VT WA WI WV WYour expansion
The agency wrote a broader phrase; these state names are ours, not theirs. Parse method nationwide, confidence high.
Food category: Dietary supplementsderived
Assigned by a reviewed keyword rulebook over the product description, not by the agency.
Recall type: Voluntary: Firm initiated
Recall number: F-0215-2014

This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.