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…
Recalling firm: New Algae Company
Why it was recalled
EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.
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Compare the exact product and package details with the label you have.
ProductEDGE, 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.
FDA code information
Lot BO1 and AO1, Expiration date Aug 2015
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Full FDA record and distribution details
Original product description
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.
Recall details
- Recall number
- F-0215-2014
- Event ID
- 66630
- FDA status
- Terminated
- Initiated
- Oct 23, 2013
- Reported
- Nov 27, 2013
- Classified
- Nov 20, 2013
- Terminated
- Mar 5, 2014
- Quantity
- 310 boxes (60 packets per box)
- Location
- Klamath Falls, OR, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Telephone
Where it was distributed
Distributed nationwide.
FDA source record · F-0215-2014
Data updated September 16, 2026. View official FDA data ↗
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