Trader Joe's Artisan Bread - Organic French Baguette; (Brown and Serve) Keep frozen; Product code 53835; 24 x 11.5 oz. (326g) - 24 loaves per case. UPC 0053 8350 Product of Canada Manufactured by Groupe Premiere Moisson Inc., 189 Harwood, Vaudreuil-Dorion, Quebec, Canada Distributed and sold exclusively by Trader Joe's, Monrovia, CA 91016
Class I - DangerousWhat Should You Do?
- Check if you have this product: Code BF118127 and BF118128; Cases codes : 53835 LOT BDUMAY-7-18 Cases codes : 53835 LOT BDUMAY-8-18
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Trader Joes Company
- Reason for Recall:
- FDA was notified by the Canadian Food Inspection Agency of that two lot codes of Trader Joe's Organic French Baguette may be contaminated with Listeria monocytogenes.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Trader Joe's Artisan Bread - Organic French Baguette; (Brown and Serve) Keep frozen; Product code 53835; 24 x 11.5 oz. (326g) - 24 loaves per case. UPC 0053 8350 Product of Canada Manufactured by Groupe Premiere Moisson Inc., 189 Harwood, Vaudreuil-Dorion, Quebec, Canada Distributed and sold exclusively by Trader Joe's, Monrovia, CA 91016
Product Codes/Lot Numbers:
Code BF118127 and BF118128; Cases codes : 53835 LOT BDUMAY-7-18 Cases codes : 53835 LOT BDUMAY-8-18
Distribution:
Distributed in: CA, PA, MA, NH, RI, ME, CT, NY, NJ, DC, VA, MD
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-1539-2018
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