CLASS III Food recall · Reported 10 Dec 2025 · FDA Enforcement Report

Coke Farm Beans, Green recalled by Triple B

Triple B is recalling Coke Farm Beans, Green, distributed in California, Minnesota, New York, Rhode Island. The recall was initiated on 29 Oct 2025 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot: 286.1831
Quantity recalled137 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-0365-2026
FDA event ID
97998
Recalling firm
Triple B, San Juan Bautista, CA
Brand
Coke
Classification
Class III
Status
Terminated
Recall initiated
29 Oct 2025
FDA classified
6 Jan 2026
Reported
10 Dec 2025
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Other Reasons
Product category
Beans & Lentils

Timeline

29 Oct 2025Recall initiated by company
10 Dec 2025Published in enforcement report+42 days
6 Jan 2026Classified by FDA+27 days

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

Reason for recall

Potential chemical contamination.

Product as listed by the FDA

COKE FARM Beans, Green 25 lb. Product of USA Coke Farm San Juan Bautista, CA 95045

Where it was distributed

U.S. Distribution: CA, MN, NY, RI

CaliforniaMinnesotaNew YorkRhode Island

Questions about this recall

Is Coke Farm Beans, Green recalled?

Yes. Triple B recalled Coke Farm Beans, Green on 29 Oct 2025. The recall is Class III and its status is Terminated. Recall number H-0365-2026.

Why was it recalled?

Potential chemical contamination.

Which lots are affected?

Lot: 286.1831

Where was it sold?

U.S. Distribution: CA, MN, NY, RI

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 21 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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