Whole Food Market Thai Shrimp Salad Serving Size
Reason Whole Food Market Spicy Harissa Salmon Salad sold in the NE region was mislabeled as Thai Shrimp Salad. This resulted in undeclared salmon (Fish) and Pistachio (treenut).
Whole Foods Markets Lobster Bisque Distributed by recall
Recalled by Whole Foods Market Northeast Regional Office · Englewood Cliffs, NJ, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Back label of Lobster Bisque product was mislabeled as Butternut Squash Soup (which contains fewer allergens [only milk] than the Lobster Bisque [milk, shellfish, wheat])
Undeclared allergens: Milk Wheat Shellfish
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 Markets Lobster Bisque Distributed by: Whole Foods Market, Englewood Cliffs, NJ 07652 UPC: 8-80632-00100
Quantity: 408 units
Food: Seafood & fish
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 16354
Where it was sold
Connecticut New Jersey New York
FDA's distribution note: CT, NJ and NY
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 milk, wheat, shellfish; 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 Northeast Regional Office
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 27, 2016
- In FDA report of
- Feb 8, 2017
- Terminated
- Feb 6, 2019
- FDA recall number
- F-1425-2017 · event 76126
- Official record
- FDA enforcement report search
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