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High RiskFDAfda-F-2898-2015OTHER

Imitation Pasteurized Process Cheese Food: BORDEN SUCREM 12/16.4OZ SANDWICH SLICES, AMER IMIT, 451101550735. COUNTRY FARE 12/10.67O...

Category
Units Affected
953,720
Recall Date
June 12, 2015
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2898-2015.

Dairy Farmers of America Inc. is recalling a number of cheese products due that a piece of plastic film strip might remain attached to the cheese slice upon peeling the film from the product.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2898-2015.

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 Dairy Farmers Of America 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-2898-2015.

Dairy Farmers OF America 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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Dairy Farmers Of America Inc Recall FAQ

Dairy Farmers Of America Inc is the subject of a dairy safety report: Imitation Pasteurized Process Cheese Food: BORDEN SUCREM 12/16.4OZ SANDWICH SLICES, AMER IMIT, 451101550735. COUNTRY FARE 12/10.67O.... The notice was published on June 12, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 953,720 units are potentially affected.