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Lower risk Food recall · FDA · Published April 25, 2017

Urban Remedy Cold Pressed Apple Juice Recall: Mislabeling Risk

Urban Remedy recalls Whole Foods Market cold pressed apple juice due to mislabeling as non-dairy spiced golden milk, which may contain tree nuts.

🇺🇸 FDA recall #F-2183-2017FoodUrban Remedy ›
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Recalling firmUrban Remedy208 S Garrard Blvd · N Richmond, CA 94801-2001
✎ GovInfoNow plain-language explainer

What happened, in plain English

Urban Remedy is recalling Whole Foods Market cold pressed apple juice that was mislabeled as non-dairy spiced golden milk. This could pose a risk for people with tree nut allergies since the product may contain tree nuts. Read more at govinfonow.com/recall/21814-urban-remedy-cold-pressed-apple-juice-recall-mislabeling-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/21814-urban-remedy-cold-pressed-apple-juice-recall-mislabeling-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-2183-2017

Cite this page

“Urban Remedy Cold Pressed Apple Juice Recall: Mislabeling Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21814-urban-remedy-cold-pressed-apple-juice-recall-mislabeling-risk. Based on FDA recall #F-2183-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2183-2017%22&limit=1).

Why it’s dangerous

The product was mislabeled as non-dairy spiced golden milk but is actually cold pressed apple juice. The ingredient list does not list tree nuts, but the mislabeling could lead to confusion and potential tree nut exposure for allergic individuals.

Who’s affected

People who purchased Whole Foods Market cold pressed apple juice (16 fl oz) with the UPC 8 13377 02154 3 are affected. Those with tree nut allergies are at higher risk due to potential mislabeling.

How to tell if you have this one

Check for the product name 'Whole Foods Market Cold Pressed Juice, Apple' with 16 fl oz (473 mL) and UPC 8 13377 02154 3. The product was sold with a best by date of May 7, 2017.

  • Brand
    Urban Remedy
  • Product
    Whole Foods Market Cold Pressed Juice, Apple; 16 FL. Oz. (1 pt) 473 mL. Keep refrigerated - Enjoy within 5 days of
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the product name 'Whole Foods Market Cold Pressed Juice, Apple' with 16 fl oz (473 mL) and UPC 8 13377 02154 3.

Where it went and when

Where it was distributed

Distributed in 3 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: not listedUTColorado: 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: “CA, NV, AZ.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, Nevada.

Recall timeline

FDA terminated this recall 36 days after the firm started it.

1. Firm started the recall: Apr 25, 201712. FDA classified it Class I: May 4, 201723. Published in FDA’s Enforcement Report: May 10, 201734. FDA terminated the recall: May 31, 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-2183-2017 (April 25, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2183-2017 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