McCain Foods USA Inc Recalls Ore-Ida Tater Tots Due to Plastic Fragments
McCain Foods USA Inc has recalled over 21,000 cases of Ore-Ida Tater Tots distributed to foodservice accounts due to potential contamination with small hard plastic fragments.
What Happened
McCain Foods USA Inc has initiated a voluntary recall of Ore-Ida Tater Tots shaped potatoes after the discovery of foreign material. The product was found to contain small, hard plastic fragments, which pose a potential physical hazard to consumers.
Which Products Are Affected
The recall involves 21,557 cases of Ore-Ida Tater Tots shaped potatoes, item number OIF00215A. The product is packaged in 30 lb cases (Net Wt. 13.6 kg), with each case containing six 5 lb clear, unlabeled poly bags.
Product Details:
- Brand/Product: Ore-Ida Tater Tots
- UPC (Case Label): 1 00 72714 00215 8
- Batch Codes: 1005475084, 1005476076, 1005477012, 1005498350
- Use By Dates: E 20271006, E 20271007, E 20271008, E 20271103
- Recall Number: H-0492-2026
This product was distributed exclusively to foodservice accounts and was not sold at retail stores. The distribution area includes the following states: AK, AL, AR, AZ, CA, CO, FL, GA, HI, ID, KS, KY, LA, MI, MN, MS, MO, NE, NM, NV, OK, OH, OR, PA, TX, UT, WA, and WI.
What You Should Do
Foodservice operators and distributors in possession of the affected batch codes should immediately stop using the product and sequester it to prevent further distribution or consumption. Affected parties should contact McCain Foods USA Inc for instructions regarding the return or disposal of the product.
Why This Matters
The presence of foreign materials, such as hard plastic fragments, in food products presents a significant safety hazard, including risks of choking or injury to the mouth and digestive tract.
Source
Information provided by the U.S. Food and Drug Administration (FDA).
Source: FDA Official Notice
Related Articles
Philips Recalls Azurion 7 M20 Systems Due to Unexpected Table Movement
FDA · February 24, 2026
Medline Industries Recalls 14 Fr Suction Catheter Kits Due to Incorrect Component Sizing
FDA · February 24, 2026
Philips Recalls Azurion 7 M12 Systems Due to Unexpected Table Movement Hazard
FDA · February 24, 2026