Product Wiki · Recalls · U.S. FDA — Food Enforcement

Recall F-0215-2014 — 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

U.S. FDA — Food Enforcement · United States · 2013-10-23 · Class I

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Agency: U.S. FDA — Food Enforcement
Recall identifier: F-0215-2014
Date of alert: 2013-10-23
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: New Algae Company
Product category: food
Product type: Food

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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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