" Product Name: Pastured Grade AA Large Eggs " Product Description: Egg Carton, 12 eggs per dozen " Pack/Julian Date(s):
Summary
The FDA issued a Class I for " Product Name: Pastured Grade AA Large Eggs " Product Description: Egg Carton, by Kenz Henz LLC. Reason: Eggs may be contaminated with Salmonella..
Details
Source
Food Recall
External ID
H-0170-2026
Action Date
2025-11-12
Status
Ongoing
Category
food
Product Description
" 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.
Lot/Code Info: 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.
Quantity Affected: 16,400 dozen
Reason for Recall
Eggs may be contaminated with Salmonella.
Distribution
Texas
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-07
Company
Santa Fe, TX
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 34 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Kenz Henz LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Kenz Henz LLC have FDA actions?
This is the only FDA action we have on record for Kenz Henz LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0170-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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