RecallHawk
Class II Recall

Idaho Pacific Fine Potato Flour, product #20501, packaged in multi-walled Kraft bag, Net Wt. 50lbs. No UPC code. Manufac

Idaho Pacific Corporation

Summary

The FDA issued a Class II for Idaho Pacific Fine Potato Flour, product #20501, packaged in multi-walled Kraft by Idaho Pacific Corporation. Reason: Potato flour item #20501 was recalled due to undeclared milk (between 13ppm and 17ppm)..

Details

Source

Food Recall

External ID

F-0573-2025

Action Date

2025-03-05

Status

Terminated

Category

food

Product Description

Idaho Pacific Fine Potato Flour, product #20501, packaged in multi-walled Kraft bag, Net Wt. 50lbs. No UPC code. Manufactured by Idaho Pacific Corporation, Ririe, ID 83443.

Lot/Code Info: Lot 241108, Bag Codes 000203 to 000283, Best By Date 5/8/2026 Lot 241109, Bag Codes 000216 to 000332, Best By Date 5/9/2026 Lot 241111, Bag Codes 000375 to 000520, Best By Date 5/11/2026

Quantity Affected: 317/50lbs. bags (total 15,850 lbs.)

Reason for Recall

Potato flour item #20501 was recalled due to undeclared milk (between 13ppm and 17ppm).

Distribution

Distributed in IL, MI, and OR.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-01-18

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

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 (Idaho Pacific Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Idaho Pacific Corporation have FDA actions?

This is the only FDA action we have on record for Idaho Pacific Corporation in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0573-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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