Skip to main content
High RiskFDAfda-F-0573-2025UNDECLARED ALLERGEN

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

Category
Units Affected
317
Recall Date
January 18, 2025
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0573-2025.

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

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0573-2025.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Idaho Pacific Corporation or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0573-2025.

Idaho Pacific Corporation

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

Visit FDA.gov →

📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

How to report to FDAFile a report at FDA

Idaho Pacific Corporation Recall FAQ

Idaho Pacific Corporation is the subject of a food safety report: Idaho Pacific Fine Potato Flour, product #20501, packaged in multi-walled Kraft bag, Net Wt. 50lbs. No UPC code. Manufactured by Idaho Pa.... The notice was published on January 18, 2025 by the U.S. Food and Drug Administration (FDA). Approximately 317 units are potentially affected.