Urban Remedy Organic Cacao Mocha Cold Brew Coffee Recall: Almond/Cashew Labeling Mix-up
Urban Remedy recalls 16 fl oz organic cacao mocha cold brew coffee due to labeling error mixing almonds and cashews. Check UPC 8 13377 02222 9 for affected products.
Lower-risk recall
Firm discovered that labeling had been switched for two products on one day of production - undeclared almonds and cashews.
Contact the company
What happened, in plain English
Urban Remedy is recalling 16 fl oz organic cacao mocha cold brew coffee because labeling was switched during production, potentially containing undeclared almonds instead of cashews. This could mislead consumers about allergens, especially for those with nut allergies. Read more at govinfonow.com/recall/14842-urban-remedy-organic-cacao-mocha-cold-brew-coffee-recall-almond.
Source Summary by GovInfoNow · govinfonow.com/recall/14842-urban-remedy-organic-cacao-mocha-cold-brew-coffee-recall-almond · Updated October 4, 2026 · FDA enforcement record: FDA #F-0330-2021
Cite this page
“Urban Remedy Organic Cacao Mocha Cold Brew Coffee Recall: Almond/Cashew Labeling Mix-up.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14842-urban-remedy-organic-cacao-mocha-cold-brew-coffee-recall-almond. Based on FDA recall #F-0330-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0330-2021%22&limit=1).
Why it’s dangerous
During production, labeling was switched for two products on one day, causing some coffee to contain undeclared almonds instead of cashews. This could lead to allergic reactions in people sensitive to nuts.
Who’s affected
Anyone who purchased Urban Remedy Organic Cacao Mocha Cold Brew Coffee with UPC 8 13377 02222 9. People with nut allergies are most at risk due to potential undeclared almonds.
How to tell if you have this one
Check for the UPC code 8 13377 02222 9 on the product label. The coffee contains cashew milk and coffee, with lot number 0391A and use by date 3/11/2021.
- Brand
Urban Remedy- Category
Food
All 2 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 II- Status
Terminated- Distribution
CA only
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-0330-2021 | Urban Remedy Organic Cacao Mocha Cold Brew Coffee; 16 FL. OZ (473 mL) UPC" 8 13377 02222 9 Ingredients: Cashew Milk (filtered water, cashew, Date syrup, Vanilla Extract, Himalayan Pink Salt) Cold Brew Coffee (filtered water, coffee bean), Cacoa Powder Contains: Cashew; Lot# 0391A Use by 3/11/2021 | 208 units |
| F-0331-2021 | Urban Remedy Organic Almond Maca Almond Milk; 16 FL. OZ (473 mL) UPC" 8 13377 02102 4 Ingredients: Almond Milk (filtered Water, Almond) Date Syrup, Vanilla Extract, Maca Root PowerCashew Milk (filtered water, cashew, Date syrup, Maca Root Powder, Himalayan Pink Salt. C Contains: Almond; Lot# 0391A Use by 3/11/2021 | 111 units |
What to do — step by step
Check Product Label
Look for the UPC code 8 13377 02222 9 and lot number 0391A on the coffee package.
Where it went and when
Where it was distributed
Distributed in California.
FDA distribution: “CA only” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California.
Recall timeline
FDA terminated this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- 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-0330-2021 (February 19, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0330-2021 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.