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Class I: serious health riskTerminated

New Algae Flex Recall

Flex, Maximum Flexibility, Item number 21-601, dietary supplement, 90 capsules per bottle

New Algae Company · Klamath Falls, OR

Risk level
Class I
Reported by FDA
Nov 27, 2013
Recall ID
F-0216-2014
Check your lot numberHow we source this data

Summary

New Algae recalled Flex starting Oct 23, 2013. The FDA classified it as Class I (serious health risk) and published enforcement report F-0216-2014 on Nov 27, 2013. Reason: Flex dietary supplement product is recalled because the finished label does not declare shark cartilage. Status: Terminated.

Why it was recalled

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

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.

Lot numbers, UPCs & expiration codes

Lot EY1, manufacturing date of 8/2013. (product expires by August 2015)

Where it was sold

Distributed nationwide.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0216-2014
Classification
Class I
Status
Terminated
Recall initiated
Oct 23, 2013
FDA report date
Nov 27, 2013
Quantity
103 bottles (90 capsules per bottle)
Recall type
Voluntary: Firm initiated
Recalling firm
New Algae Company

Original FDA data

Every field from FDA enforcement report F-0216-2014, exactly as published.

Show all FDA fields
City
Klamath Falls
State
OR
Status
Terminated
Country
United States
Event ID
66630
Address
565 Century Ct
Code information
Lot EY1, manufacturing date of 8/2013. (product expires by August 2015)
Postal code
97601-7100
Report date
Nov 27, 2013
Product type
Food
Recall number
F-0216-2014
Classification
Class I
Recalling firm
New Algae Company
Product quantity
103 bottles (90 capsules per bottle)
Termination date
Mar 5, 2014
Reason for recall
Flex dietary supplement product is recalled because the finished label does not declare shark cartilage.
Voluntary / mandated
Voluntary: Firm initiated
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.
Distribution pattern
Distributed nationwide.
Recall initiation date
Oct 23, 2013
Initial firm notification
Telephone
Center classification date
Nov 20, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0216-2014, published Nov 27, 2013. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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