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Stop using now Food recall · FDA · Published May 28, 2018

Trader Joe's Organic French Baguette Recall: Listeria Contamination Risk

Trader Joe's recalls 24-pack of Organic French Baguette (Product Code 53835) due to potential Listeria monocytogenes contamination. Consumers should discard frozen items immediately.

🇺🇸 FDA recall #F-1539-2018FoodTrader Joe's ›
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Recalling firmTrader Joes Company800 S Shamrock Ave · Monrovia, CA 91016-6346
✎ GovInfoNow plain-language explainer

What happened, in plain English

Trader Joe's is recalling 24 packs of Organic French Baguette that may contain Listeria monocytogenes. This bacteria can cause serious illness, so affected products should be discarded immediately. Read more at govinfonow.com/recall/19090-trader-joe-s-organic-french-baguette-recall-listeria-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/19090-trader-joe-s-organic-french-baguette-recall-listeria-contamination-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-1539-2018

Cite this page

“Trader Joe's Organic French Baguette Recall: Listeria Contamination Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19090-trader-joe-s-organic-french-baguette-recall-listeria-contamination-risk. Based on FDA recall #F-1539-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1539-2018%22&limit=1).

Why it’s dangerous

Listeria monocytogenes is a bacteria that can cause serious infections, especially in pregnant women, newborns, and people with weakened immune systems. Contaminated bread may lead to foodborne illness if eaten after thawing.

Who’s affected

Anyone who purchased Trader Joe's Organic French Baguette with Product Code 53835 from Canada. People with weakened immune systems are at higher risk for severe illness.

How to tell if you have this one

Check for Product Code 53835 on the packaging. The product is a 24-pack of 11.5 oz. Organic French Baguette (Brown and Serve) that must be kept frozen. Cases were sold with lot codes BDUMAY-7-18 and BDUMAY-8-18.

  • Brand
    Trader Joe's
  • Product
    Trader Joe's Artisan Bread - Organic French Baguette; (Brown and Serve) Keep frozen; Product code 53835; 24 x 11.5 oz
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Discard Frozen Products

    Immediately throw away all 24 packs of Organic French Baguette with Product Code 53835 that were sold with lot codes BDUMAY-7-18 or BDUMAY-8-18.

Where it went and when

Where it was distributed

Distributed in 11 states and D.C..

Alaska: not listedAKMaine: yesMEVermont: not listedVTNew Hampshire: yesNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: yesDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Distribution Centers in CA and PA - retail locations in MA, NH, RI, ME, CT, NY, NJ, DC, PA, VA, MD.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Connecticut, District of Columbia, Maine, Maryland, Massachusetts, New Hampshire, New Jersey, New York, Pennsylvania, Rhode Island, Virginia.

Recall timeline

FDA terminated this recall 35 days after the firm started it.

1. Firm started the recall: May 28, 201812. FDA classified it Class II: Jun 7, 201823. Published in FDA’s Enforcement Report: Jun 13, 201834. FDA terminated the recall: Jul 2, 201842018
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1539-2018 (May 28, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1539-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA