Brians Cauliflower 83 oz Imported by EUROPEAN NATURAL FOOD & TRADING CO. Inc, 72 Lehigh Avenue Paterson, NJ 07593 UPC 858567002421
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1082-2016.
Brian's Cauliflower may contain undeclared sulfites.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1082-2016.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact European Natural Foods & Trading Company, Inc. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1082-2016.
European Natural Foods & Trading Company, Inc.
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
European Natural Foods & Trading Company, Inc. Recall FAQ
European Natural Foods & Trading Company, Inc. is the subject of a food safety report: Brians Cauliflower 83 oz Imported by EUROPEAN NATURAL FOOD & TRADING CO. Inc, 72 Lehigh Avenue Paterson, NJ 07593 UPC 858567002421. The notice was published on January 26, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 300 units are potentially affected.