CLASS I Food recall · Reported 30 Oct 2019 · FDA Enforcement Report

Samosa Cauli Wrap recalled by Urban Remedy

Urban Remedy is recalling Samosa Cauli Wrap, distributed in California. The recall was initiated on 11 Sep 2019 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUse by 9/15/2019
Quantity recalled189 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0066-2020
FDA event ID
83785
Recalling firm
Urban Remedy, North Richmond, CA
Classification
Class I
Status
Terminated
Recall initiated
11 Sep 2019
FDA classified
23 Oct 2019
Reported
30 Oct 2019
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
E. coli
Product category
Dumplings

Timeline

11 Sep 2019Recall initiated by company
23 Oct 2019Classified by FDA+42 days
30 Oct 2019Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Random sampling of spinach from vendor found Enterohemorrhagic E-Coli/Shiga Toxin Producing E. Coli.

Some strains of E. coli, such as O157:H7, produce a toxin that can cause severe stomach cramps, bloody diarrhea and, in a small number of cases, kidney failure.

Product as listed by the FDA

Samosa Cauli Wrap; 6.7 oz. UPC: 813377 023097

Where it was distributed

CA only

California

Questions about this recall

Is Samosa Cauli Wrap recalled?

Yes. Urban Remedy recalled Samosa Cauli Wrap on 11 Sep 2019. The recall is Class I and its status is Terminated. Recall number F-0066-2020.

Why was it recalled?

Random sampling of spinach from vendor found Enterohemorrhagic E-Coli/Shiga Toxin Producing E. Coli.

Which lots are affected?

Use by 9/15/2019

Where was it sold?

CA only

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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