Drug recall
EDGE, Item number 21-620, dietary supplement, 60 packet per box. The Edge product includes two different…
FDA recall event 66630 · Class I · New Algae Company
Key facts
| Event ID | 66630 |
|---|---|
| Recall numbers | F-0215-2014, F-0216-2014 |
| Recalling firm | New Algae Company |
| Product type | Food |
| Products | 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…, Flex, Maximum Flexibility, Item number 21-601, dietary supplement, 90 capsules per bottle. The Flex product is a dietary supplement in capsule form containing vegetable glucosamine HCL, chondroitin… |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage., Flex dietary supplement product is recalled because the finished label does not declare shark cartilage. |
| Initiation date | Oct 23, 2013 |
| Report date | Nov 27, 2013 |
| Termination date | Mar 5, 2014 |
| City | Klamath Falls |
| State | OR |
| Country | United States |
| FEI number | 3022187 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: