Egg Salad Sandwich
Reason Almark Foods issued recall for potential Listeria monocytogenes in ingredient used by firm's supplier.
GREAT AMERICAN DELI PREMIUM CHICKEN SALAD WHEATBERRRY sandwiches… recall
Recalled by Great American Deli, LLC · Ooltewah, TN, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product contains undeclared eggs and soy.
Undeclared allergens: Egg Soy
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
GREAT AMERICAN DELI PREMIUM CHICKEN SALAD WHEATBERRRY sandwiches are packaged in a flexible plastic containers, NET WT. 6.4 oz (181g), Great American Deli, PO Box 27, Ooltewah, TN 37363 UPC 7 41431 00228 6
Quantity: 816 sandwiches
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot number 17 198
Where it was sold
Georgia Kentucky Michigan Tennessee
FDA's distribution note: Product was distributed in Michigan, Kentucky, Tennessee and Georgia.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to egg, soy; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Great American Deli, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 6, 2017
- In FDA report of
- Nov 1, 2017
- Terminated
- Feb 28, 2019
- FDA recall number
- F-0039-2018 · event 78241
- Official record
- FDA enforcement report search
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