RecallHawk
Class II Recall

Good & Gather Cut Green Beans. Net Wt. 14.5 oz (411g). UPC 0 85239-11628 9. Dist. By Target Corporation, Minneapolis,

Del Monte Foods, Inc

Summary

The FDA issued a Class II for Good & Gather Cut Green Beans. Net Wt. 14.5 oz (411g). UPC 0 85239-11628 9. D by Del Monte Foods, Inc. Reason: Foreign Object.

Details

Source

Food Recall

External ID

F-0627-2025

Action Date

2025-03-19

Status

Terminated

Category

food

Product Description

Good & Gather Cut Green Beans. Net Wt. 14.5 oz (411g). UPC 0 85239-11628 9. Dist. By Target Corporation, Minneapolis, MN 55403.

Lot/Code Info: Best if Used By 28 OCT 2026, Lot 7AA 418507

Quantity Affected: 8,242cases (24cans/case)

Reason for Recall

Foreign Object

Distribution

AL, AZ, CA, CO, GA, IA, IL, IN, KS, MI, MN, NC, NJ, NY, OH, OR, PA, SC, TX, VA, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2025-02-12

Company

Del Monte Foods, Inc

Walnut Creek, CA

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

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

Del Monte Foods, Inc has 3 FDA actions in our database, including 3 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (Del Monte Foods, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Del Monte Foods, Inc have FDA actions?

Del Monte Foods, Inc has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0627-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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