CLASS II Food recall · Reported 28 May 2014 · FDA Enforcement Report

Bolivian Artichoke Salad recalled by Whole Foods Market Group

Whole Foods Market Group is recalling Bolivian Artichoke Salad, distributed in Connecticut, Massachusetts, New Jersey, New York, Rhode Island. The recall was initiated on 29 Apr 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesSell By : 05/02/2014

Quantity recalled190 lbs.

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-1951-2014
FDA event ID: 68166
Recalling firm: Whole Foods Market Group, Everett, MA
Brand: Bolivian Artichoke
Classification: Class II
Status: Terminated
Recall initiated: 29 Apr 2014
FDA classified: 20 May 2014
Reported: 28 May 2014
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Foreign Material
Product category: Salad Kits

Timeline

29 Apr 2014	Recall initiated by company
20 May 2014	Classified by FDA	+21 days
28 May 2014	Published in enforcement report	+8 days

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

Reason for recall

Potential for foreign material -glass

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Bolivian Artichoke Salad sold at Whole Foods 10 lb bulk bags, refrigerated

Where it was distributed

CT, MA, NJ, NY, RI

Connecticut Massachusetts New Jersey New York Rhode Island

Stores named: Whole Foods

Questions about this recall

Why was it recalled?

Potential for foreign material -glass

Which lots are affected?

Sell By : 05/02/2014

Where was it sold?

CT, MA, NJ, NY, RI

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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