RecallHawk
Class III Recall

Black Beans, Dried, net wt. 16 OZ (1 LB) 454g, packaged in plastic bag. Packaged in the U.S. UPC 0 70552 70412 1. DISTRI

Trinidad Benham Corp

Summary

The FDA issued a Class III for Black Beans, Dried, net wt. 16 OZ (1 LB) 454g, packaged in plastic bag. Packaged by Trinidad Benham Corp. Reason: Elevated levels of MBC (carbendazim) thiophanate-methyl..

Details

Source

Food Recall

External ID

F-0665-2025

Action Date

2025-03-19

Status

Terminated

Category

food

Product Description

Black Beans, Dried, net wt. 16 OZ (1 LB) 454g, packaged in plastic bag. Packaged in the U.S. UPC 0 70552 70412 1. DISTRIBUTED BY: WinCo Foods, LLC, BOISE, ID 83704

Lot/Code Info: BEST IF USED BY 07OCT25 W Code interpreted as follows: 07: Day of Month Produced OCT: Month Produced 25: Year produced plus 1 W: Plant designator = Moses Lake, WA

Quantity Affected: 504 cases

Reason for Recall

Elevated levels of MBC (carbendazim) thiophanate-methyl.

Distribution

Distributed in AZ, CA, ID, and OR.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-02-11

Company

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 55 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Trinidad Benham Corp has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Trinidad Benham Corp) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Trinidad Benham Corp have FDA actions?

Trinidad Benham Corp has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0665-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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