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High RiskFDAfda-F-0824-2018LISTERIA

IQF Green beans, sold as Not Ready To Eat (NRTE) product for use in foodservice or manufacturing applications. The product cases are labe...

Category
Units Affected
14,235
Recall Date
January 19, 2018
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0824-2018.

Frozen green beans are recalled due to a potential contamination with Listeria monocytogenes.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0824-2018.

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 National Frozen Foods Corporation--seattle 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-0824-2018.

National Frozen Foods Corporation--Seattle

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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National Frozen Foods Corporation--seattle Recall FAQ

National Frozen Foods Corporation--seattle is the subject of a food safety report: IQF Green beans, sold as Not Ready To Eat (NRTE) product for use in foodservice or manufacturing applications. The product cases are labe.... The notice was published on January 19, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 14,235 units are potentially affected.