The Recall Desk

FDA (Food) recall action 66630

New Algae Company recalled 2 products on 2013-11-27

The FDA (Food) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2013-11-27
Critical
0
Units
—

Why these products were recalled

Flex dietary supplement product is recalled because the finished label does not declare shark cartilage.

EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.

The agency’s own wording, quoted from the enforcement report.

1–2 of 2

  • HighFDA (Food)··2013-11-27

    Flex Dietary Supplement Recalled for Undeclared Shark Cartilage

    New Algae Company is recalling Flex dietary supplement bottles because the label fails to declare shark cartilage, a potential allergen.

    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 ca
    Category
    Distribution
    0 states
  • HighFDA (Food)··2013-11-27

    New Algae Company Recalls EDGE Dietary Supplement for Undeclared Shark Cartilage

    New Algae Company is recalling EDGE dietary supplement packets because the label fails to declare shark cartilage. The product was distributed nationwide.

    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
    Category
    Distribution
    0 states