RecallHawk
Class II Recall

Woodland Gourmet Arrowroot Flour item code H59EE86, Net Wt. 55 lb., bag in box

Woodland Foods LLC

Summary

The FDA issued a Class II for Woodland Gourmet Arrowroot Flour item code H59EE86, Net Wt. 55 lb., bag in box by Woodland Foods LLC. Reason: Possible presence of Foreign Material.

Details

Source

Food Recall

External ID

H-0515-2026

Action Date

2026-02-25

Status

Terminated

Category

food

Product Description

Woodland Gourmet Arrowroot Flour item code H59EE86, Net Wt. 55 lb., bag in box

Lot/Code Info: LOT ID 2479025 2478961 2490352 2495607 2494472 2495650 2495529 2495593

Quantity Affected: 30,030lbs

Reason for Recall

Possible presence of Foreign Material

Distribution

KY

Type: Voluntary: Firm initiated

Recall Initiated: 2026-01-16

Company

Woodland Foods LLC

Waukegan, IL

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 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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

How often does Woodland Foods LLC have FDA actions?

Woodland Foods LLC 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 "H-0515-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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