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Lower risk Food recall · FDA · Published October 4, 2016

Del Monte Light Sliced Peaches Mislabeled as Fruit Cocktail - Recall

Del Monte recalls 15oz Yellow Cling Peaches that were mislabeled as Fruit Cocktail in Heavy Syrup, containing cherry-colored carmine. This allergen requires FDA labeling per regulations.

🇺🇸 FDA recall #F-0279-2017FoodDel Monte ›
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Recalling firmDel Monte Research Center - Walnut Creek205 N Wiget Ln · Walnut Creek, CA 94598-2403
✎ GovInfoNow plain-language explainer

What happened, in plain English

Del Monte is recalling 15-ounce yellow cling peaches that were mislabeled as containing fruit cocktail in heavy syrup instead of the stated 'Lite Sliced Peaches.' This mislabeling means the product contains carmine, a cherry-colored food dye that requires allergen labeling under FDA rules. Read more at govinfonow.com/recall/23068-del-monte-light-sliced-peaches-mislabeled-as-fruit-cocktail-recall.

Source Summary by GovInfoNow · govinfonow.com/recall/23068-del-monte-light-sliced-peaches-mislabeled-as-fruit-cocktail-recall · Updated October 9, 2026 · FDA enforcement record: FDA #F-0279-2017

Cite this page

“Del Monte Light Sliced Peaches Mislabeled as Fruit Cocktail - Recall.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23068-del-monte-light-sliced-peaches-mislabeled-as-fruit-cocktail-recall. Based on FDA recall #F-0279-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0279-2017%22&limit=1).

Why it’s dangerous

The product was mislabeled as 'Lite Sliced Peaches' but actually contains fruit cocktail in heavy syrup, which includes carmine. Carmine is a red dye derived from insects and is a known allergen that requires FDA labeling under food safety regulations.

Who’s affected

People who purchased the recalled 15-ounce yellow cling peaches from Del Monte between August 15, 2015 and August 14, 2018. Those with carmine allergies are at risk due to the mislabeled product containing the dye.

How to tell if you have this one

Check for the product name 'DM Light Slices Yellow Cling Peaches -15 oz (425g) 300 x 407' with lot number 522701 and manufacture date August 15, 2015. The best by date is August 14, 2018.

  • Brand
    Del Monte
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the lot number 522701 and manufacture date of August 15, 2015 on the can.

Where it went and when

Where it was distributed

Distributed in 4 states.

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: yesNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: yesUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew 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: “AZ, CA, NV, UT” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, Nevada, Utah.

Recall timeline

FDA terminated this recall 9 months after the firm started it.

1. Firm started the recall: Oct 4, 201612. FDA classified it Class II: Oct 25, 201623. Published in FDA’s Enforcement Report: Nov 2, 201634. FDA terminated the recall: Jul 20, 2017420162017
  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-0279-2017 (October 4, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0279-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 9, 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