Aleia's Classic Croutons
Reason Product manufactured with cumin that may contain peanut protein.
Aleia's Parmesan Croutons recall
Recalled by Aleias Gluten Free Foods LLC · Branford, CT, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Product manufactured with cumin that may contain peanut protein.
Undeclared allergen: Peanut
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
Aleia's Parmesan Croutons, Gluten Free, NET WT 8 oz (226.8g). UPC Code: 8 55930 00162 3, Product is packaged in a brown cardboard box with white text.
Quantity: 628 cases
Food: Cheese
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 Numbers: 410221, 413121, 416021, 417221, 419221, 510110, 514210
Where it was sold
California Connecticut Massachusetts Maine New Hampshire New Jersey New York Texas
FDA's distribution note: Product was distributed in the following states: TX, MA, ME, CT, CA, NH, NY, TX, NJ
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. The risk from an undeclared allergen is to people allergic to peanut; 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
- Aleias Gluten Free Foods LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 29, 2015
- In FDA report of
- May 20, 2015
- Terminated
- Oct 3, 2018
- FDA recall number
- F-2204-2015 · event 70394
- 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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