EDGE — Class I food recall F-0215-2014
Terminated recall by New Algae Company, reported 2013-11-27, distributed nationwide. EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.
| Recall number | F-0215-2014 |
|---|---|
| Product type | Food |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | New Algae Company, Klamath Falls, OR, United States |
| Recall initiated | 2013-10-23 |
| Classified | 2013-11-20 |
| Reported by FDA | 2013-11-27 |
| Terminated | 2014-03-05 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| Lot numbers | AO1, BO1 |
| Model numbers | 21-620 |
| Expiration dates | 2015-08-20 |
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.
Reason for recall
EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-0215-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.