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-

FDA recall notice · announced November 27, 2013 · New Algae

Class I FDA/FSIS Class I: reasonable probability that use will cause serious adverse health consequences or death.

The 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.

Reason for recall

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

Notes

Distribution: Distributed nationwide.
Lot/code information: Lot EY1, manufacturing date of 8/2013. (product expires by August 2015)
Quantity: 103 bottles (90 capsules per bottle)
Status: Terminated
Products in this recall event:
- 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 (F-0215-2014)
- 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 su (F-0216-2014)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.