CLASS I ONGOING Food recall · Reported 23 Sep 2026 · FDA Enforcement Report

Organic Triple Berry Blend Strawberries, Blackberries & Blueberries recalled

Frutas y Hortalizas del Sur is recalling Organic Triple Berry Blend Strawberries, Blackberries & Blueberries, distributed in Arkansas. The recall was initiated on 28 Aug 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot 6 040 01-6 Best by Date Feb 09 2028
Quantity recalled3,026 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
H-1380-2026
FDA event ID
99831
Recalling firm
Frutas y Hortalizas del Sur, San Carlos, N/A
Classification
Class I
Status
Ongoing
Recall initiated
28 Aug 2026
FDA classified
16 Sep 2026
Reported
23 Sep 2026
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
E. coli
Product category
Strawberries

Timeline

28 Aug 2026Recall initiated by company
16 Sep 2026Classified by FDA+19 days
23 Sep 2026Published 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 E. coli O145:H28 Contamination

Some strains of E. coli, such as O157:H7, produce a toxin that can cause severe stomach cramps, bloody diarrhea and, in a small number of cases, kidney failure.

Product as listed by the FDA

Organic Triple Berry Blend Strawberries, Blackberries & Blueberries, NET WT 10 OZ (283g), packed in plastic bag, 5 bags per case of 10 OZ each. KEEP FROZEN

Where it was distributed

AR

Arkansas

Questions about this recall

Why was it recalled?

Potential E. coli O145:H28 Contamination

Which lots are affected?

Lot 6 040 01-6 Best by Date Feb 09 2028

Where was it sold?

AR

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 29 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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