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CriticalFDAfda-F-0678-2020LISTERIA

Premo Turkey & Cheese on a Pretzel Sub Bun, 7 oz., UPC: 612510094037

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
203,881
Recall Date
January 6, 2020
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0678-2020.

Products recalled due to potential contamination with Listeria monocytogenes

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0678-2020.

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 Lipari Foods Operating Company, 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-0678-2020.

Lipari Foods Operating Company, LLC.

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.

How to report to FDAFile a report at FDA

Lipari Foods Operating Company, Llc. Recall FAQ

Lipari Foods Operating Company, Llc. is the subject of a dairy safety report: Premo Turkey & Cheese on a Pretzel Sub Bun, 7 oz., UPC: 612510094037. The notice was published on January 6, 2020 by the U.S. Food and Drug Administration (FDA). Approximately 203,881 units are potentially affected.