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High RiskFDAfda-F-0377-2018CONTAMINATION

Little Caesar's Family Meal Kits, Paper cartons, Contains: 1 pizza crust( 12 x 16), 1 package of pizza sauce, 1 package of cheese, 1 pack...

Category
Units Affected
97,104
Recall Date
October 6, 2017
Issuing Agency
Hazard
Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0377-2018.

Champion Foods, LLC is voluntarily conducting a recall of multiple brands of Cheesy Bread sticks, Italian Bread sticks, bread kits and pizza kits following a supplier's recall of ingredient due to potential physical contaminants from an ink pen.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0377-2018.

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 Champion Foods, Llc 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-0377-2018.

Champion Foods, LLC

FDA

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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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Champion Foods, Llc Recall FAQ

Champion Foods, Llc is the subject of a dairy safety report: Little Caesar's Family Meal Kits, Paper cartons, Contains: 1 pizza crust( 12 x 16), 1 package of pizza sauce, 1 package of cheese, 1 pack.... The notice was published on October 6, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 97,104 units are potentially affected.