" Product Name: Pastured Grade AA Large Eggs " Product Description:…

Kenz Henz LLC has recalled " Product Name: Pastured Grade AA Large Eggs " Product Description:…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on November 12, 2025 and was initiated on October 7, 2025. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers " Product Name: Pastured Grade AA Large Eggs " Product Description:…, with approximately 16,400 dozen affected. The company behind the recall is Kenz Henz LLC, based in Santa Fe, TX. The FDA describes the product as: “" Product Name: Pastured Grade AA Large Eggs " Product Description: Egg Carton, 12 eggs per dozen " Pack/Julian Date(s): Julian date 241(Aug 30) to 244 (Sep 2) and 246 (Sep 4) to 247 (Sep 5), Best by Dates 10/11 to 10/14/25 and 10/16 to 10/17.”

Why was " Product Name: Pastured Grade AA Large Eggs " Product Description:… recalled?

According to the FDA, the stated reason for the recall is: “Eggs may be contaminated with Salmonella.” In plain terms, this recall relates to Salmonella.

Salmonella is a group of bacteria that is one of the most common causes of foodborne illness in the United States. Public health authorities note that infections can lead to symptoms such as fever, diarrhea, and stomach cramps, and that young children, older adults, and people with weakened immune systems are at higher risk of serious illness. Because it can spread through contaminated food, regulators treat Salmonella findings seriously.

What should you do?

If you think you may have bought " Product Name: Pastured Grade AA Large Eggs " Product Description:…, compare it against the product description and identifying codes (Julian date 241(Aug 30) to 244 (Sep 2) and 246 (Sep 4) to 247 (Sep 5), Best by Dates 10/11 to 10/14/25 and 10/16 to 10/17.) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Kenz Henz LLC or your local health authority.

About this recall

This recall was distributed in TX. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.