Agave Dream Cappuccino Recall: Listeria Contamination Risk
Agave Dream recalls 1-pint cappuccino with potential Listeria monocytogenes contamination. Affected products sold between July 2017 and December 2017. Consumers should check UPC code 8 9934900204 8.
Lower-risk recall
Potential Listeria monocytogenes contamination.
Contact the company
What happened, in plain English
Agave Dream is recalling 1-pint cappuccino products that may contain Listeria monocytogenes. This bacteria can cause serious illness, especially for pregnant women, newborns, and those with weakened immune systems. Read more at govinfonow.com/recall/22887-agave-dream-cappuccino-recall-listeria-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/22887-agave-dream-cappuccino-recall-listeria-contamination-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-0603-2017
Cite this page
“Agave Dream Cappuccino Recall: Listeria Contamination Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22887-agave-dream-cappuccino-recall-listeria-contamination-risk. Based on FDA recall #F-0603-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0603-2017%22&limit=1).
Why it’s dangerous
Listeria monocytogenes is a bacteria that can cause serious infections in vulnerable groups. It spreads through contaminated food and can lead to miscarriage, stillbirth, or severe illness in newborns.
Who’s affected
Pregnant women, newborns, and people with weakened immune systems are at higher risk from Listeria. Most consumers are unlikely to be affected unless they consumed the recalled product.
How to tell if you have this one
Check for Agave Dream Cappuccino 1 Pint with UPC code 8 9934900204 8. Products were sold from July 2017 through December 2017.
- Brand
Agave Dream- Product
Agave Dream Cappuccino 1 Pint UPC Code 8 9934900204 8- Category
Food
All 5 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
U.S. distribution to the following; CA, OR, IL, TX, IN, SC, NJ, WA. No foreign distribution.
| Recall number | Product, codes & lots |
|---|---|
| F-0601-2017 | Agave Dream Lavender 1 Pint UPC Code 8 9934900206 2; Dates: 12/2/17 |
| F-0602-2017 | Agave Dream Chocolate Chip 1 Pint UPC Code 8 9934900302 1; Dates: 8/5/17, 12/12/17 |
| F-0603-2017 | Agave Dream Cappuccino 1 Pint UPC Code 8 9934900204 8; Dates: 7/4/17, 9/9/17, 12/2/17 |
| F-0604-2017 | Agave Dream Chocolate 1 Pint UPC Code 8 9934900202 4; Dates: 7/4/17, 8/5/17, 9/9/17, 10/9/17, 12/12/17, 12/24/17 |
| F-0605-2017 | Agave Dream Vanilla 1 Pint UPC Code 8 9934900201 7; Dates: 7/4/17, 9/9/17,10/9/17, 12/12/17, 7/14/18 |
What to do — step by step
Check Product UPC
Look for the UPC code 8 9934900204 8 on the product label.
Where it went and when
Where it was distributed
Distributed in 8 states.
FDA distribution: “U.S. distribution to the following; CA, OR, IL, TX, IN, SC, NJ, WA. No foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Illinois, Indiana, New Jersey, Oregon, South Carolina, Texas, Washington.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Is this product safe to drink?
The recall indicates potential Listeria contamination, so it is not safe to consume. The product should be discarded.
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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-0603-2017 (November 10, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0603-2017 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.