The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A hardy bacteria that can grow at refrigerator temperatures and cause severe illness in vulnerable groups.
Action required
Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent.
Product distributed in Arkansas, California, Florida, Georgia, Indiana, Louisiana, Maryland, Missouri, New York, Ohio, Pennsylvania, Tennessee, Texas, Virginia
United States
Quantity affected
1366 cases
Recall initiation
FDA report date: July 3, 2024
FDA recall number
F-1405-2024
Beyond the headline
The recall, in context
Classic Delight LLC initiated this food recall on June 10, 2024. The FDA enforcement report states: Possibly contaminated with Listeria monocytogenes. The FDA report lists distribution as: Product distributed in Arkansas, California, Florida, Georgia, Indiana, Louisiana, Maryland, Missouri, New York, Ohio, Pennsylvania, Tennessee, Texas, Virginia.
The FDA enforcement report describes the reason as: Possibly contaminated with Listeria monocytogenes
(Item 806604) Wakefield Ham, Egg & Cheese Muffin was made or distributed by Classic Delight LLC in Saint Marys, OH, United States. This page reflects FDA report F-1405-2024, dated July 3, 2024.
Why this is a Class II recall
Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a hardy bacteria that can grow at refrigerator temperatures and cause severe illness in vulnerable groups.
FDA definition
The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.
What to do now
1
Stop using it
Do not eat, drink or take the affected product.
2
Check the codes
Compare the lot and date codes against the table above.
3
Return or discard
Contact the retailer or recalling firm about a refund, and dispose of the product safely.
Consumer safety guide
Listeria monocytogenes
Symptoms to watch for
Fever, muscle aches, nausea and diarrhea may occur. Severe infection can cause headache, stiff neck, confusion, loss of balance or convulsions.
When symptoms may appear
Symptoms can begin within a few days, but can take up to several weeks to appear.
Higher-risk groups
Pregnant people, newborns, adults over 65 and immunocompromised people are at the highest risk of severe illness.
What to do now
1Stop using or eating the affected product and keep it away from children and pets.
2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
3If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.
General guidance based on CDC and FDA consumer information.
This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.
Frequently asked
Questions about this recall
4 answers
What is the (Item 806604) Wakefield Ham, Egg & Cheese Muffin recall?
Classic Delight LLC recalled (Item 806604) Wakefield Ham, Egg & Cheese Muffin in an FDA Class II enforcement action reported as F-1405-2024. Possibly contaminated with Listeria monocytogenes
What should I do if I bought this product?
Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent. Stop using or eating the affected product and keep it away from children and pets. Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer. If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.
Is the Classic Delight LLC recall still active?
The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.
Where can I verify this recall?
This page is normalized from the openFDA enforcement record F-1405-2024. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.
Verify before you act.
VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.