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Lower risk Food recall · FDA · Published September 11, 2019

Urban Remedy Samosa Cauli Wrap Recall: E. Coli Risk

Urban Remedy recalls 6.7 oz. Samosa Cauli Wrap (UPC 813377 023097) due to potential E. Coli contamination. Stop using if you have this product.

🇺🇸 FDA recall #F-0066-2020FoodUrban Remedy ›
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Recalling firmUrban Remedy208 S Garrard Blvd · North Richmond, CA 94801-2001
✎ GovInfoNow plain-language explainer

What happened, in plain English

Urban Remedy is recalling 6.7 oz. Samosa Cauli Wrap (UPC 813377 023097) because random spinach samples from the vendor tested positive for harmful E. Coli bacteria. This could cause foodborne illness if eaten. Read more at govinfonow.com/recall/16659-urban-remedy-samosa-cauli-wrap-recall-e-coli-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/16659-urban-remedy-samosa-cauli-wrap-recall-e-coli-risk · Updated October 5, 2026 · FDA enforcement record: FDA #F-0066-2020

Cite this page

“Urban Remedy Samosa Cauli Wrap Recall: E. Coli Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16659-urban-remedy-samosa-cauli-wrap-recall-e-coli-risk. Based on FDA recall #F-0066-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0066-2020%22&limit=1).

Why it’s dangerous

The spinach used in the product was found to contain harmful E. Coli bacteria during random sampling. This type of bacteria can cause food poisoning if the product is consumed.

Who’s affected

Anyone who purchased the Samosa Cauli Wrap with UPC 813377 023097 before its use-by date of September 15, 2019. People who eat the product are at risk of foodborne illness.

How to tell if you have this one

Check for the product name 'Samosa Cauli Wrap' and UPC code 813377 023097. The product was sold until September 15, 2019, with a use-by date of that date.

  • Brand
    Urban Remedy
  • Product
    Samosa Cauli Wrap; 6.7 oz. UPC: 813377 023097
  • Category
    Food
FDA recall event · 4 products

All 4 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
    CA only
Recall numberProduct, codes & lotsQuantity
F-0064-2020Black Rise Umeboshi Bowl; 12 oz. UPC: 813377 022595; Use by 9/15/2019241 units
F-0065-2020The Benedict Brunch Bowl; 9.7 oz. UPC: 813377 022854; Use by 9/15/2019120 units
F-0066-2020Samosa Cauli Wrap; 6.7 oz. UPC: 813377 023097; Use by 9/15/2019189 units
F-0067-2020Green Tea Leaf Salad 6.7 oz. UPC: 813377 023158; Use by 9/15/2019unknown
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the UPC code 813377 023097 on the Samosa Cauli Wrap packaging.

Where it went and when

Where it was distributed

Distributed in California.

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: not listedNVWyoming: 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: not listedAZNew 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 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 56 days after the firm started it.

1. Firm started the recall: Sep 11, 201912. FDA classified it Class I: Oct 23, 201923. Published in FDA’s Enforcement Report: Oct 30, 201934. FDA terminated the recall: Nov 6, 201942019
  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-0066-2020 (September 11, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0066-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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