F-0216-2014 Class I Terminated
FDA food recall F-0216-2014 was initiated by New Algae Company on October 23, 2013 and is designated Class I. Reason for recall: Flex dietary supplement product is recalled because the finished label does not declare shark cartilage. The recall status is terminated (terminated March 5, 2014). Affected quantity: 103 bottles (90 capsules per bottle).
Recall Details
- Product Type
- Food
- Report Date
- November 27, 2013
- Initiation Date
- October 23, 2013
- Termination Date
- March 5, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 103 bottles (90 capsules per bottle)
Product 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.
Reason for Recall
Flex dietary supplement product is recalled because the finished label does not declare shark cartilage.
Distribution Pattern
Distributed nationwide.
Code Information
Lot EY1, manufacturing date of 8/2013. (product expires by August 2015)