Drug recall
Echinacea Agustifolia PE 4& echinosides The product is in powder form extracted from the Echinacea root packed…
FDA recall event 68530 · Class III · Naturex Inc.
Key facts
| Event ID | 68530 |
|---|---|
| Recall numbers | F-2177-2014, F-2178-2014, F-2179-2014 |
| Recalling firm | Naturex Inc. |
| Product type | Food |
| Products | Echinacea Agustifolia PE 4& echinosides The product is in powder form extracted from the Echinacea root packed in varying size lined cardboard boxes containing 10 kg or 25 kg., Echinacea Agustifolia Root PE 4:1 The product is in powder form extracted from the Echinacea root packed in varying size lined cardboard boxes containing 10 kg or 25 kg., Echinacea Angustifolia Root PE 4: The product is in powder form extracted from the Echinacea root packed in varying size lined cardboard boxes containing 10 kg or 25 kg. |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507. |
| Initiation date | Jun 9, 2014 |
| Report date | Jul 23, 2014 |
| Termination date | Nov 14, 2014 |
| City | S Hackensack |
| State | NJ |
| Country | United States |
| FEI number | 2210504 |
At a glance
- 1–9 Products in this recall
- 10–99 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: