CLASS II Food recall · Reported 25 Nov 2020 · FDA Enforcement Report

FC Tomatoes Roma Diced 3/8" 1/5# recalled by FreshPoint Dallas

FreshPoint Dallas is recalling FC Tomatoes Roma Diced 3/8" 1/5#; FC Tomatoes Roma Diced 3/8" 4/5#, and FC Tomatoes Roma, distributed in Kansas, Texas. The recall was initiated on 20 Oct 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLOT CODE: 7420286
Quantity recalled142 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-0119-2021
FDA event ID
86683
Recalling firm
FreshPoint Dallas, Dallas, TX
Classification
Class II
Status
Terminated
Recall initiated
20 Oct 2020
FDA classified
18 Nov 2020
Reported
25 Nov 2020
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Foreign Material
Product category
Tomatoes

Timeline

20 Oct 2020Recall initiated by company
18 Nov 2020Classified by FDA+29 days
25 Nov 2020Published in enforcement report+7 days

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

Reason for recall

Potential Foreign Material

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

FC TOMATOES ROMA DICED 3/8" 1/5#; FC TOMATOES ROMA DICED 3/8" 4/5#, and FC TOMATOES ROMA DICED 3/8" 2/5# all packaged in white plastic trays with heat seal lid, packed inside a cardboard box

Where it was distributed

Texas and Kansas

KansasTexas

Questions about this recall

Why was it recalled?

Potential Foreign Material

Which lots are affected?

LOT CODE: 7420286

Where was it sold?

Texas and Kansas

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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