CLASS I Food recall · Reported 12 Mar 2014 · FDA Enforcement Report

Whole (round) Tomatoes recalled by Big Red Tomato Packers

BIG RED Tomato Packers is recalling Whole (round) Tomatoes, distributed in Florida, Michigan, Minnesota, North Carolina, Pennsylvania, Tennessee. The recall was initiated on 7 Feb 2014 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codes1106
Quantity recalled790 Boxes

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-1604-2014
FDA event ID
67460
Recalling firm
BIG RED Tomato Packers, Fort Pierce, FL
Classification
Class I
Status
Terminated
Recall initiated
7 Feb 2014
FDA classified
4 Mar 2014
Reported
12 Mar 2014
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Salmonella
Product category
Tomatoes

Timeline

7 Feb 2014Recall initiated by company
4 Mar 2014Classified by FDA+25 days
12 Mar 2014Published 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

Positive Salmonella finding

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Whole (round) Tomatoes packed in cardboard boxes of 20 and 25 lbs each.

Where it was distributed

FL, MI, MN, NC, PA and TN

FloridaMichiganMinnesotaNorth CarolinaPennsylvaniaTennessee

Questions about this recall

Why was it recalled?

Positive Salmonella finding

Which lots are affected?

1106

Where was it sold?

FL, MI, MN, NC, PA and TN

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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