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High RiskFDAfda-F-0180-2016LACERATION

Frozen Corn distributed under the following labels and sizes: (a) WYLWOOD Super Sweet Whole Kernel Corn, NET WT. 16 OZ (1 LB), UPC 05193...

Category
Units Affected
9,335
Recall Date
August 28, 2015
Issuing Agency
Hazard
Laceration

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0180-2016.

One code of Wylwood brand Frozen Whole Kernel Corn was found to be contaminated with Listeria monocytogenes based on sampling and analysis by the State of Tennessee. The firm decided to recall other labels and codes produced the same day as the suspect lot as a precaution.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0180-2016.

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 Bonduelle Usa 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-0180-2016.

Bonduelle USA Inc

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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Bonduelle Usa Inc Recall FAQ

Bonduelle Usa Inc is the subject of a produce safety report: Frozen Corn distributed under the following labels and sizes: (a) WYLWOOD Super Sweet Whole Kernel Corn, NET WT. 16 OZ (1 LB), UPC 05193.... The notice was published on August 28, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 9,335 units are potentially affected.