Simplot¿ Traditional Reduced Sodium Tater Gems¿

JR Simplot Company has recalled Simplot¿ Traditional Reduced Sodium Tater Gems¿, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on December 17, 2025 and was initiated on November 18, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Simplot¿ Traditional Reduced Sodium Tater Gems¿, with approximately 7053 cases (6/5lb. bags per case) affected. The company behind the recall is JR Simplot Company, based in Boise, ID. The FDA describes the product as: “Simplot¿ Traditional Reduced Sodium Tater Gems¿ , formed frozen potatoes, 6/5lb bags per case, foodservice item, master case UPC 100 71179 00418 9. Distributed by Simplot Global Food, LLC, P.O. Box 9386, Boise, ID 83707”

Why was Simplot¿ Traditional Reduced Sodium Tater Gems¿ recalled?

According to the FDA, the stated reason for the recall is: “Plastic fragments. Pieces of semi-rigid plastic embedded in the recalled Tater Gems product.” In plain terms, this recall relates to foreign material.

A foreign material recall means that pieces of something which should not be in food — such as metal, plastic, or glass — may be present. These can pose a choking hazard or cause injury. Recalls like these are issued to remove the affected product before anyone is hurt.

What should you do?

If you think you may have bought Simplot¿ Traditional Reduced Sodium Tater Gems¿, compare it against the product description and identifying codes (Lot Code: 087 FEB 16 25 1 Lot Interpretation: 087 - Production Facility FEB - Production Month 16 - Production Date 25 - Production Year 1 Line of Production) before using it.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact JR Simplot Company or your local health authority.

About this recall

This recall was distributed in ID. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.