FindMyRecallSubscribe
Class I: serious health riskTerminated

New Algae Edge Recall

EDGE, Item number 21-620, dietary supplement, 60 packet per box

New Algae Company · Klamath Falls, OR

Risk level
Class I
Reported by FDA
Nov 27, 2013
Recall ID
F-0215-2014
Check your lot numberHow we source this data

Summary

New Algae recalled Edge starting Oct 23, 2013. The FDA classified it as Class I (serious health risk) and published enforcement report F-0215-2014 on Nov 27, 2013. Reason: EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage. Status: Terminated.

Why it was recalled

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

Product description

EDGE, Item number 21-620, dietary supplement, 60 packet per box. The Edge product includes two different packets of capsules - a "Before" packet and an "After" packet. The suggested use for the After packet is one packet (or 6 capsules) per day. The suggested use for the "Before" packet is one packet (or 4 capsules) per day.

Lot numbers, UPCs & expiration codes

Lot BO1 and AO1, Expiration date Aug 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-0215-2014
Classification
Class I
Status
Terminated
Recall initiated
Oct 23, 2013
FDA report date
Nov 27, 2013
Quantity
310 boxes (60 packets per box)
Recall type
Voluntary: Firm initiated
Recalling firm
New Algae Company

Original FDA data

Every field from FDA enforcement report F-0215-2014, 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 BO1 and AO1, Expiration date Aug 2015
Postal code
97601-7100
Report date
Nov 27, 2013
Product type
Food
Recall number
F-0215-2014
Classification
Class I
Recalling firm
New Algae Company
Product quantity
310 boxes (60 packets per box)
Termination date
Mar 5, 2014
Reason for recall
EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.
Voluntary / mandated
Voluntary: Firm initiated
Product description
EDGE, Item number 21-620, dietary supplement, 60 packet per box. The Edge product includes two different packets of capsules - a "Before" packet and an "After" packet. The suggested use for the After packet is one packet (or 6 capsules) per day. The suggested use for the "Before" packet is one packet (or 4 capsules) 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-0215-2014, published Nov 27, 2013. View the source record (openFDA) · FDA enforcement reports

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

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions.

How we source and update recall data · Report incorrect information

Other recent food recalls