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High RiskFDAfda-F-0132-2020CONTAMINATION

Market Choice Monster Cheeseburger, Net Wt. 9.1 oz individually wrapped in plastic, packaged 12 count per case.

Category
Units Affected
633
Recall Date
October 29, 2019
Issuing Agency
Hazard
Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0132-2020.

The firm received a recall notice for an ingredient, ready-to-eat beef patties, which were potentially contaminated with foreign metal material. The patties were used in the manufacture of sandwiches.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0132-2020.

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 Pride Of Iowa Sandwiches, Inc. 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-0132-2020.

Pride of Iowa Sandwiches, Inc.

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.

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📣 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.

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Pride Of Iowa Sandwiches, Inc. Recall FAQ

Pride Of Iowa Sandwiches, Inc. is the subject of a dairy safety report: Market Choice Monster Cheeseburger, Net Wt. 9.1 oz individually wrapped in plastic, packaged 12 count per case.. The notice was published on October 29, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 633 units are potentially affected.