Whole Foods Mesclun Goat Cheese Salad Mini
Reason Product labels switched and undeclared allergens not declared in ingredient statement. Caesar salad contains undeclared tree nuts and Goat Cheese salad undeclared fish
Whole Foods Caesar Salad Mini recall
Recalled by Whole Foods Market Group Inc. · Everett, MA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product labels switched and undeclared allergens not declared in ingredient statement. Caesar salad contains undeclared tree nuts and Goat Cheese salad undeclared fish
Undeclared allergens: Tree nuts Fish
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
Whole Foods Caesar Salad Mini Net Wt 4 0z plastic shell
Quantity: 592 units
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.
Sell By 7/11/14
Where it was sold
Connecticut New Jersey New York
FDA's distribution note: CT, NY, NJ
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 tree nuts, fish; 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
- Whole Foods Market Group Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 8, 2014
- In FDA report of
- Aug 6, 2014
- Terminated
- Jul 30, 2014
- FDA recall number
- F-2238-2014 · event 68726
- 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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