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Unrated Food recall · FDA · Published November 27, 2020

Landert Multigrain Solene Figotte Bread Recall: Unapproved Pesticide Risk

Landert LLC recalls prebaked frozen multigrain breads with sesame seeds due to unapproved pesticide-ethylene oxide from India. Consumers should check product labels for Lot #1234567 and contact Landert for details.

🇺🇸 FDA recall #F-0190-2021FoodLandert ›
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Contact the company

Recalling firmLandert LLC6041 Copper Leaf Ln · Naples, FL 34116-6719
✎ GovInfoNow plain-language explainer

What happened, in plain English

Landert LLC is recalling prebaked frozen multigrain breads with sesame seeds because they contain unapproved pesticide-ethylene oxide from India. This could pose a health risk if consumed, so affected consumers should stop using the product. Read more at govinfonow.com/recall/15000-landert-multigrain-solene-figotte-bread-recall-unapproved-pesticide-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/15000-landert-multigrain-solene-figotte-bread-recall-unapproved-pesticide-risk · Updated October 4, 2026 · FDA enforcement record: FDA #F-0190-2021

Cite this page

“Landert Multigrain Solene Figotte Bread Recall: Unapproved Pesticide Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/15000-landert-multigrain-solene-figotte-bread-recall-unapproved-pesticide-risk. Based on FDA recall #F-0190-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0190-2021%22&limit=1).

Why it’s dangerous

The breads contain unapproved pesticide-ethylene oxide from India, which was used in the production of flour for the breads. This chemical is not approved for use in food products and could pose health risks if consumed.

Who’s affected

Anyone who owns or uses Landert's Multigrain Solene Figotte breads with sesame seeds. People who consume the breads are at risk of potential health effects from the unapproved pesticide.

How to tell if you have this one

Check for the product name 'Multigrain Solene Figotte', item number 29497, lot number 1234567, and best before date 11/19/21 on the packaging.

  • Brand
    Landert
  • Product
    Multigrain Solene Figotte, prebaked frozen breads with seeds, Item 29497, Net Weight 8.8 Lbs (4 Kg), Lot: 1234567, UPC
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the lot number 1234567 and best before date 11/19/21 on the packaging.

Where it went and when

Where it was distributed

Distributed in Florida.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “Distributed to 5 consignees in FL” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida.

Recall timeline

FDA terminated this recall 5 months after the firm started it.

1. Firm started the recall: Nov 27, 202012. FDA classified it Class II: Dec 31, 202023. Published in FDA’s Enforcement Report: Jan 6, 202134. FDA terminated the recall: May 12, 2021420202021
  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-0190-2021 (November 27, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0190-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 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