Severity
Critical
CriticalClass ITerminated
FDA Food recall · Reported November 27, 2013
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.
EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.
Compiled from official public sources by the editorial team.
Verify with FDA Food →
New Algae Company recalled EDGE, Item number 21-620, dietary supplement, 60 packet per box. The Edge product incl… - a critical-severity action.
EDGE, Item number 21-620, dietary supplement, 60 packet per box. The Edge product incl… was recalled by New Algae Company in November 27, 2013. Reason: EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.. Check the official notice for the remedy. Verify recall #F-0215-2014 with the FDA Food before acting.
The recall
New Algae Company issued this critical-severity FDA Food recall-EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage..
- Critical
- severity level
- Class I
- classification
- November 27, 2013
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0215-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0215-2014) was formally reported on November 27, 2013, with the manufacturer initiating the action on October 23, 2013. It is classified under Critical severity (Class I), with a current status of Terminated. New Algae Company is listed as the recalling firm, operating out of Klamath Falls, OR. Federal records list the affected scope as 310 boxes (60 packets per box).
The documented reason for this recall is: EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage. Distribution data in the federal record shows the product reached: Distributed nationwide.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
310 boxes (60 packets per box)
Related Recalls
6
6 from same agency
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.
Reason for recall
EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-0215-2014 |
| Date reported | November 27, 2013 |
| Date initiated | October 23, 2013 |
| Recalling firm | New Algae Company |
| Firm location | Klamath Falls, OR |
| Affected scope | 310 boxes (60 packets per box) |
| Distribution | Distributed nationwide. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0215-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by New Algae Company. Units affected: 310 boxes (60 packets per box).
Why was this product recalled? ▼
EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on November 27, 2013. Severity: Critical. Recall number: F-0215-2014.
Where was the recalled product distributed? ▼
Distribution: Distributed nationwide..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0215-2014) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported November 27, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.