CLASS II Food recall · Reported 11 May 2016 · FDA Enforcement Report

La Fiesta Bean Salad Tubs) Made By Fresh Creative Foods recalled

Vaughan Foods is recalling La Fiesta Bean Salad Tubs) Made By Fresh Creative Foods Moore, OK 73160, distributed in Iowa, Illinois, Indiana, Missouri, Wisconsin. The recall was initiated on 4 Apr 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesProduct ID #: 402690; Best if Used By: 05/07/2016, Lot: BFEGJD and Best if Used By: 05/11/2016, Lot: BFGHFE
Quantity recalled126 cases

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-1319-2016
FDA event ID
73762
Recalling firm
Vaughan Foods, Moore, OK
Classification
Class II
Status
Terminated
Recall initiated
4 Apr 2016
FDA classified
5 May 2016
Reported
11 May 2016
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Product category
Salad Kits

Timeline

4 Apr 2016Recall initiated by company
5 May 2016Classified by FDA+31 days
11 May 2016Published 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

Undeclared Wheat.

Product as listed by the FDA

La Fiesta Bean Salad (2/5 LB Tubs) Made By Fresh Creative Foods Moore, OK 73160 UPC 013454371763 packaged in white plastic tub with lid

Where it was distributed

MO, IL, IN, WI, and IA

IowaIllinoisIndianaMissouriWisconsin

Questions about this recall

Why was it recalled?

Undeclared Wheat.

Which lots are affected?

Product ID #: 402690; Best if Used By: 05/07/2016, Lot: BFEGJD and Best if Used By: 05/11/2016, Lot: BFGHFE

Where was it sold?

MO, IL, IN, WI, and IA

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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