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Lower risk Food recall · FDA · Published April 13, 2017

Del Monte Caesar Side Salad Recall: Undeclared Allergens in 3 oz Packaging

Del Monte recalls 7-ELEVEN Caesar Side Salad 3 oz containers due to undeclared milk, eggs, wheat and fish (anchovies). Consumers should check UPC 052548594145 and lot 07101101 for affected items.

🇺🇸 FDA recall #F-2204-2017FoodDel Monte ›
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Recalling firmDel Monte Fresh Produce N.A., Inc. HQ241 Sevilla Ave · Coral Gables, FL 33134-6622
✎ GovInfoNow plain-language explainer

What happened, in plain English

Del Monte is recalling 7-ELEVEN Caesar Side Salad 3 oz packages because they contain undeclared allergens including milk, eggs, wheat, and fish (anchovies). This affects people with allergies to these ingredients, who could experience allergic reactions if they consume the product. Read more at govinfonow.com/recall/21863-del-monte-caesar-side-salad-recall-undeclared-allergens-in-3.

Source Summary by GovInfoNow · govinfonow.com/recall/21863-del-monte-caesar-side-salad-recall-undeclared-allergens-in-3 · Updated October 8, 2026 · FDA enforcement record: FDA #F-2204-2017

Cite this page

“Del Monte Caesar Side Salad Recall: Undeclared Allergens in 3 oz Packaging.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21863-del-monte-caesar-side-salad-recall-undeclared-allergens-in-3. Based on FDA recall #F-2204-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2204-2017%22&limit=1).

Why it’s dangerous

The product contains undeclared allergens that could cause allergic reactions in sensitive individuals. The presence of these ingredients without proper labeling means people with allergies might unknowingly consume them.

Who’s affected

People with allergies to milk, eggs, wheat, or fish (anchovies) are at risk. Those who purchased the product from 7-ELEVEN stores between April 2017 and the best-by date are most likely affected.

How to tell if you have this one

Check for the product name '7-ELEVEN CAESAR SIDE SALAD 3 oz' in clear plastic containers. Look for UPC 052548594145 and lot number 07101101 on the packaging.

  • Brand
    Del Monte
  • Product
    7-ELEVEN CAESAR SIDE SALAD 3 oz. packaged in clear plastic container
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the UPC 052548594145 and lot number 07101101 on the container.

Where it went and when

Where it was distributed

Distributed in Colorado.

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: yesCONebraska: 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: not listedFL

FDA distribution: “The product is sold only in 7-11 stores in Colorado.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Colorado.

Recall timeline

FDA terminated this recall 2 months after the firm started it.

1. Firm started the recall: Apr 13, 201712. FDA classified it Class I: May 8, 201723. Published in FDA’s Enforcement Report: May 17, 201734. FDA terminated the recall: Jun 14, 201742017
  1. Firm started the recall
  2. FDA classified it Class I
  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-2204-2017 (April 13, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2204-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 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