EDGE Dietary Supplement (New Algae Company) – undeclared shark cartilage (2013)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
New Algae Company
Lot Codes / Batch Numbers
Lot BO1 and AO1, Expiration date Aug 2015
Products Sold
Lot BO1 and AO1, Expiration date Aug 2015
New Algae Company is recalling EDGE, Item number 21-620, dietary supplement, 60 packet per box. The Edge product includes two di due to EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 6, 2026