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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Food

New Algae Company: EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.; Flex dietary supplement product is recalled because the finished label does not declare shark cartilage.

Agency Publication Date: November 20, 2013
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Affected Products

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.

Lot BO1 and AO1, Expiration date Aug 2015

Lot Numbers:
BO1
Product: Flex, Maximum Flexibility, Item number 21-601, dietary supplement, 90 capsules per bottle. The Flex product is a dietary supplement in capsule form containing vegetable glucosamine HCL, chondroitin sulfate (shark cartilage), organic microalgae (aph. flos-aquae) and chicken cartilage. The serving size is 3 capsules and the suggested use is one 3 capsule serving per day.

Lot EY1, manufacturing date of 8/2013. (product expires by August 2015)

Lot Numbers:
EY1

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 66630
Status: Resolved
Manufacturer: New Algae Company
Manufactured In: United States
Units Affected: 2 products (310 boxes (60 packets per box); 103 bottles (90 capsules per bottle))

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.