Echinacea Angustifolia Root PE 4: The product is in recall
Echinacea Angustifolia Root PE 4: The product is in powder form extracted from the Echinacea root packed in varying size lined cardboard boxes…
Why was Echinacea Angustifolia Root PE 4: The product is in recalled?
Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
EC330955, Lot#C073/050/A14
- Product
- Echinacea Angustifolia Root PE 4: The product is in powder form extracted from the Echinacea root packed in varying size lined cardboard boxes…
- Recalling firm
- Naturex Inc.
- Quantity
- 25 kg
- Distribution
- TN, TX, & WA
- Recall date
- July 23, 2014
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (food)