Home / Food recalls / 2013
New Algae Company
FDA recall F-0215-2014 · Class I · reported 2013-11-27 · Terminated
- Product
- 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.
- Reason
- EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.
- Quantity
- 310 boxes (60 packets per box)
- Distribution
- Distributed nationwide.
- Firm location
- OR, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Telephone
- Recall started
- 2013-10-23
- Terminated
- 2014-03-05
- Code info
- Lot BO1 and AO1, Expiration date Aug 2015
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.