CLASS I Food recall · Reported 20 Dec 2023 · FDA Enforcement Report

Malichita Whole Cantaloupe recalled by Pacific Trellis Fruit

Pacific Trellis Fruit is recalling Malichita Whole Cantaloupe, distributed in California, Illinois, Oklahoma, Texas, Wisconsin. The recall was initiated on 24 Nov 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesPLU Lot Code 4050 21651 4050 21699 4050 21775 4050 21787 4050 21870
Quantity recalled4,872 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-0579-2024
FDA event ID
93487
Recalling firm
Pacific Trellis Fruit, Los Angeles, CA
Classification
Class I
Status
Terminated
Recall initiated
24 Nov 2023
FDA classified
13 Dec 2023
Reported
20 Dec 2023
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
Melons

Timeline

24 Nov 2023Recall initiated by company
13 Dec 2023Classified by FDA+19 days
20 Dec 2023Published 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

Salmonella

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

Malichita brand Whole Cantaloupe 9 count and 12 count

Where it was distributed

U.S. distribution to the following: WI, OK, IL, TX, CA Foreign distribution to the following: Canada

CaliforniaIllinoisOklahomaTexasWisconsin

Questions about this recall

Why was it recalled?

Salmonella

Which lots are affected?

PLU Lot Code 4050 21651 4050 21699 4050 21775 4050 21787 4050 21870

Where was it sold?

U.S. distribution to the following: WI, OK, IL, TX, CA Foreign distribution to the following: Canada

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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