CLASS I Food recall · Reported 8 Nov 2023 · FDA Enforcement Report

FreshPoint Bix Produce Company, Cantaloupe recalled

Bix Produce is recalling FreshPoint Bix Produce Company, Cantaloupe, distributed in Iowa, Minnesota, North Dakota, Wisconsin. The recall was initiated on 29 Sep 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBix Lot Numbers: P2742702-00 and P2741287
Quantity recalled61 - 3 packs

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-0304-2024
FDA event ID
93162
Recalling firm
Bix Produce, Little Canada, MN
Classification
Class I
Status
Terminated
Recall initiated
29 Sep 2023
FDA classified
30 Oct 2023
Reported
8 Nov 2023
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Salmonella
Product category
Melons

Timeline

29 Sep 2023Recall initiated by company
30 Oct 2023Classified by FDA+31 days
8 Nov 2023Published 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

Cantaloupe may be contaminated with 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

FreshPoint Bix Produce Company, Cantaloupe. Item # 03143. 3 melons per bag.

Where it was distributed

IA, MN, ND, WI

IowaMinnesotaNorth DakotaWisconsin

Questions about this recall

Why was it recalled?

Cantaloupe may be contaminated with Salmonella.

Which lots are affected?

Bix Lot Numbers: P2742702-00 and P2741287

Where was it sold?

IA, MN, ND, WI

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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