Legendary Baking of Denver, CO is recalling 726 Private Selection 9-inch pies labeled as "Apple Lattice" with a UPC of 1111060195 and Lot Code 12296 (located on side of aluminum…
Health risk
The product has a reasonable probability of causing serious adverse health consequences or death. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.
Action required
Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.
Distributed to Quality Food Centers (QFC) in Washington State and Oregon by common carrier.
United States
Quantity affected
726 pies
Recall initiation
FDA report date: December 12, 2012
FDA recall number
F-0805-2013
Beyond the headline
The recall, in context
Legendary Baking initiated this food recall on November 21, 2012. The FDA enforcement report states: Legendary Baking of Denver, CO is recalling 726 Private Selection 9-inch pies labeled as "Apple Lattice" with a UPC of 1111060195 and Lot Code 12296 (located on side of aluminum pie tie) because the pies may contain undeclared EGGS. People who have an allergy or severe sensitivity to EGGS may run the risk of serious or life-threatening allergic reaction if they consume these products. The FDA report lists distribution as: Distributed to Quality Food Centers (QFC) in Washington State and Oregon by common carrier.
The FDA enforcement report describes the reason as: Legendary Baking of Denver, CO is recalling 726 Private Selection 9-inch pies labeled as "Apple Lattice" with a UPC of 1111060195 and Lot Code 12296 (located on side of aluminum pie tie) because the pies may contain undeclared EGGS. People who have an allergy or severe sensitivity to EGGS may run the risk of serious or life-threatening allergic reaction if they consume these products.
Apple Lattice Pie (9-inch, 36oz) was made or distributed by Legendary Baking in Chaska, MN, United States. This page reflects FDA report F-0805-2013, dated December 12, 2012.
Why this is a Class I recall
Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.
FDA definition
The product has a reasonable probability of causing serious adverse health consequences or death.
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
Undeclared allergen
Symptoms to watch for
Hives, swelling, wheezing, coughing, vomiting, abdominal pain or a drop in blood pressure. Anaphylaxis is a medical emergency.
When symptoms may appear
Allergic reactions often begin within minutes to a few hours of eating the allergen.
Higher-risk groups
Anyone with a diagnosed food allergy, especially children, and people with a history of anaphylaxis or asthma.
What to do now
1Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy.
2If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services.
3Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.
For a severe allergic reaction, do not wait for a callback or refund process before seeking emergency care.
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
8 answers
What is the Apple Lattice Pie (9-inch, 36oz) recall?
Legendary Baking recalled Apple Lattice Pie (9-inch, 36oz) in an FDA Class I enforcement action reported as F-0805-2013. Legendary Baking of Denver, CO is recalling 726 Private Selection 9-inch pies labeled as "Apple Lattice" with a UPC of 1111060195 and Lot Code 12296 (located on side of aluminum…
What are the symptoms of Undeclared allergen exposure?
Hives, swelling, wheezing, coughing, vomiting, abdominal pain or a drop in blood pressure. Anaphylaxis is a medical emergency.
How quickly can Undeclared allergen symptoms appear?
Allergic reactions often begin within minutes to a few hours of eating the allergen.
Who is most at risk from Undeclared allergen?
Anyone with a diagnosed food allergy, especially children, and people with a history of anaphylaxis or asthma.
What should I do if I bought this product?
Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy. If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services. Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.
How do I get a refund from Legendary Baking?
Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-0805-2013 and keep the packaging, lot code and proof of purchase if you have them.
Is the Legendary Baking 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-0805-2013. 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.