EDGE, Item number 21-620, dietary supplement, 60 packet per box. The Edge product includes two…
Recalling firm: New Algae Company
EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 5, 2014.
Check your package
Compare the exact product and package details with the label you have.
FDA code information
Lot BO1 and AO1, Expiration date Aug 2015
Match the product, package size, and code together. A missing match does not guarantee safety.
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.
Original FDA recall reason
EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.
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.
Data updated September 16, 2026. View official FDA data ↗
Follow official FDA and manufacturer guidance.