CLASS I Food recall · Reported 10 May 2017 · FDA Enforcement Report

Whole Foods Market Cold Pressed Juice, Apple recalled by Urban Remedy

Urban Remedy is recalling Whole Foods Market Cold Pressed Juice, Apple, distributed in Arizona, California, Nevada. The recall was initiated on 25 Apr 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest by May 7, 2017
Quantity recalled656 bottles - 16 fl oz.

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-2183-2017
FDA event ID
77157
Recalling firm
Urban Remedy, N Richmond, CA
Classification
Class I
Status
Terminated
Recall initiated
25 Apr 2017
FDA classified
4 May 2017
Reported
10 May 2017
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Labeling Errors
Product category
Juice

Timeline

25 Apr 2017Recall initiated by company
4 May 2017Classified by FDA+9 days
10 May 2017Published in enforcement report+6 days

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

Reason for recall

Urban Remedy is voluntarily recalling Non-Dairy Spiced Golden Milk that was mislabeled as cold pressed apple juice. The ingredient list does not list tree nuts.

Product as listed by the FDA

Whole Foods Market Cold Pressed Juice, Apple; 16 FL. Oz. (1 pt) 473 mL. Keep refrigerated - Enjoy within 5 days of opening. UPC 8 13377 02154 3

Where it was distributed

CA, NV, AZ.

ArizonaCaliforniaNevada

Stores named: Whole Foods

Questions about this recall

Why was it recalled?

Urban Remedy is voluntarily recalling Non-Dairy Spiced Golden Milk that was mislabeled as cold pressed apple juice. The ingredient list does not list tree nuts.

Which lots are affected?

Best by May 7, 2017

Where was it sold?

CA, NV, AZ.

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 26 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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