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.

Class I - Dangerous
Recalled: October 23, 2013 New Algae Company Meat & Poultry Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot EY1, manufacturing date of 8/2013. (product expires by August 2015)
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
New Algae Company
Reason for Recall:
Flex dietary supplement product is recalled because the finished label does not declare shark cartilage.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

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.

Product Codes/Lot Numbers:

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

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0216-2014

Related Recalls