Class ITerminated in FDA datasetOct 23, 2013

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,…

Recalling firm: New Algae Company

Why it was recalled

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

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Compare the exact product and package details with the label you have.

ProductFlex, 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.

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.

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.

FDA source record · F-0216-2014

Data updated September 16, 2026. View official FDA data ↗

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