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.
The exact 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.
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
Lot EY1, manufacturing date of 8/2013. (product expires by August 2015)
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 ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.