Flex, Maximum Flexibility, Item number 21-601, dietary supplement, 90 capsules per bottle. The…
Recalling firm: New Algae Company
Flex dietary supplement product is recalled because the finished label does not declare shark cartilage.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 5, 2014.
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FDA code information
Lot EY1, manufacturing date of 8/2013. (product expires by August 2015)
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Full FDA record and distribution details
Original 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.
Original FDA recall reason
Flex dietary supplement product is recalled because the finished label does not declare shark cartilage.
Recall details
- Recall number
- F-0216-2014
- Event ID
- 66630
- FDA status
- Terminated
- Initiated
- Oct 23, 2013
- Reported
- Nov 27, 2013
- Classified
- Nov 20, 2013
- Terminated
- Mar 5, 2014
- Quantity
- 103 bottles (90 capsules per bottle)
- Location
- Klamath Falls, OR, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Telephone
Where it was distributed
Distributed nationwide.
Data updated September 16, 2026. View official FDA data ↗
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