Corn Tortillas
Reason Tortillas Tita initiated a voluntary recall of all lots of their Corn Tortillas and Tortilla Enchilada produced between September 2016 and December 7, 2016, due to undeclared allergen Wheat.
Tortilla Enchilada recall
Recalled by Tortillas Tita, LLC · Wayne, MI, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Tortillas Tita initiated a voluntary recall of all lots of their Corn Tortillas and Tortilla Enchilada produced between September 2016 and December 7, 2016, due to undeclared allergen Wheat.
Undeclared allergen: Wheat
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
Tortilla Enchilada, 16 Oz. /16 units per case, packed in plastic bags
Quantity: 25 boxes
Food: Bread & bakery
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.
UPC: 0865168000039, 16 Oz. /16 units per case; All lots produced between September 2016 and December 7, 2016.
Where it was sold
Michigan Ohio Virginia
FDA's distribution note: Domestic: MI, OH Foreign: None VA/DOD: None
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to wheat; 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
- Tortillas Tita, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 8, 2016
- In FDA report of
- Feb 1, 2017
- Terminated
- May 30, 2017
- FDA recall number
- F-1355-2017 · event 76176
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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