CLASS I Food recall · Reported 15 May 2019 · FDA Enforcement Report

fresh cut cantaloupe and fresh cut mixed fruit recalled by Caito Foods

Caito Foods is recalling fresh cut cantaloupe and fresh cut mixed fruit containing one of these melons. The recall was initiated on 12 Apr 2019 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest by or Use by 4/19/2019 and any date prior
Quantity recalled279,205 retail units

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-1338-2019
FDA event ID
82623
Recalling firm
Caito Foods, Indianapolis, IN
Classification
Class I
Status
Terminated
Recall initiated
12 Apr 2019
FDA classified
9 May 2019
Reported
15 May 2019
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Salmonella
Product category
Melons

Timeline

12 Apr 2019Recall initiated by company
9 May 2019Classified by FDA+27 days
15 May 2019Published 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

Potential to be contaminated with Salmonella Carrau

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

Fresh cut watermelon, fresh cut honeydew melon, fresh cut cantaloupe and fresh cut mixed fruit containing one of these melons.

Where it was distributed

see below.

Questions about this recall

Why was it recalled?

Potential to be contaminated with Salmonella Carrau

Which lots are affected?

Best by or Use by 4/19/2019 and any date prior

Where was it sold?

see below.

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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