EchoLakeFoods MF 3067 CNFREE Cage Free Precooked IAF Scrambled Eggs Net Wt. 28 lbs. Bulk. Keep Frozen. Manufactured b
Summary
The FDA issued a Class I for EchoLakeFoods MF 3067 CNFREE Cage Free Precooked IAF Scrambled Eggs Net Wt. 28 by Echo Lake Foods, Inc.. Reason: Potential Listeria monocytogenes contamination..
Details
Source
Food Recall
External ID
H-0168-2026
Action Date
2025-11-05
Status
Terminated
Category
food
Product Description
EchoLakeFoods MF 3067 CNFREE Cage Free Precooked IAF Scrambled Eggs Net Wt. 28 lbs. Bulk. Keep Frozen. Manufactured by: Echo Lake Foods, Inc., 2319 Raymond Ave. Franksville, WI 53126.
Lot/Code Info: Lot number 5164. Expiration Date December 13, 2026
Quantity Affected: 824 - 28 lb Cases (23,072 lbs. total)
Reason for Recall
Potential Listeria monocytogenes contamination.
Distribution
CA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-23
Company
Franksville, WI
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 62 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 (Echo Lake Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Echo Lake Foods, Inc. have FDA actions?
This is the only FDA action we have on record for Echo Lake Foods, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0168-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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