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Stop using now Food recall · FDA · Published July 19, 2016

Agave Dream Cappuccino Ice Cream Recalled for Listeria Risk

Agave Dream recalls Cappuccino Ice Cream Pints due to potential Listeria monocytogenes contamination. Check your UPC and best-by date.

🇺🇸 FDA recall #F-1969-2016FoodAgave Dream ›
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Recalling firmAgave Dream4823 Oakwood Ave · La Canada, CA 91011-2541
✎ GovInfoNow plain-language explainer

What happened, in plain English

Agave Dream is recalling its Cappuccino Ice Cream Pint because of a potential Listeria monocytogenes contamination. The affected product has the UPC code 899349002048 and a Best By date of 07/04/17. This recall covers 396 cases distributed in California, Oregon, Illinois, South Carolina, and Indiana. Read more at govinfonow.com/recall/23787-agave-dream-cappuccino-ice-cream-recalled-for-listeria-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/23787-agave-dream-cappuccino-ice-cream-recalled-for-listeria-risk · Updated October 9, 2026 · FDA enforcement record: FDA #F-1969-2016

Cite this page

“Agave Dream Cappuccino Ice Cream Recalled for Listeria Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23787-agave-dream-cappuccino-ice-cream-recalled-for-listeria-risk. Based on FDA recall #F-1969-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1969-2016%22&limit=1).

Why it’s dangerous

Listeria monocytogenes is a bacterium that can cause serious infections, particularly for pregnant women, newborns, the elderly, and people with weakened immune systems. Consumption of contaminated ice cream can lead to listeriosis, which may result in fever, muscle aches, and gastrointestinal symptoms.

Who’s affected

Consumers who purchased Agave Dream Cappuccino Ice Cream Pints with UPC code 899349002048 and a Best By date of 07/04/17 in California, Oregon, Illinois, South Carolina, or Indiana.

How to tell if you have this one

Check your ice cream pint for the UPC code 899349002048 and a Best By date of 07/04/17. The product was distributed to stores in California, Oregon, Illinois, South Carolina, and Indiana.

  • Brand
    Agave Dream
  • Product
    Agave Dream Cappuccino Ice Cream Pint UPC code: 899349002048
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the Agave Dream Cappuccino Ice Cream Pint if it matches the recalled UPC and best-by date.

  2. Discard or return the item

    The recall record does not specify a remedy, so you should discard the product or contact the retailer for a refund.

Where it went and when

Where it was distributed

Distributed in 5 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: yesINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: 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: yesSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “U.S. distribution to the following; CA, OR, IL, SC, IN. No foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Illinois, Indiana, Oregon, South Carolina.

Recall timeline

FDA terminated this recall 7 months after the firm started it.

1. Firm started the recall: Jul 19, 201612. FDA classified it Class I: Aug 23, 201623. Published in FDA’s Enforcement Report: Aug 31, 201634. FDA terminated the recall: Feb 13, 2017420162017
  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-1969-2016 (July 19, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1969-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b 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