CLASS I Food recall · Reported 18 Dec 2013 · FDA Enforcement Report

Dawn's Vidalia Onion Dip recalled

Dawn's Foods is recalling Dawn's Vidalia Onion Dip, distributed in Wisconsin. The recall was initiated on 11 Nov 2013 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUse By: 11/27/13 - 1/15/14

Quantity recalled189 cases (2-5 lb containers per case)

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-0721-2014
FDA event ID: 66831
Recalling firm: Dawn's Foods, Portage, WI
Brand: Dawn's Vidalia
Classification: Class I
Status: Terminated
Recall initiated: 11 Nov 2013
FDA classified: 9 Dec 2013
Reported: 18 Dec 2013
Type: Voluntary: Firm initiated
Customers notified by: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category: Undeclared Egg
Product category: Dips & Spreads

Timeline

11 Nov 2013	Recall initiated by company
9 Dec 2013	Classified by FDA	+28 days
18 Dec 2013	Published in enforcement report	+9 days

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

Reason for recall

Dawn's Foods is recalling Vandellia Onion Dip due to undeclared egg.

Product as listed by the FDA

Dawn's Vidalia Onion Dip, Net Wt. 5 lbs. (2.27 kg)

Where it was distributed

WI only

Wisconsin

Questions about this recall

Why was it recalled?

Dawn's Foods is recalling Vandellia Onion Dip due to undeclared egg.

Which lots are affected?

Use By: 11/27/13 - 1/15/14

Where was it sold?

WI 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 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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