Food Recall Check
Class I · High risk Terminated Initiated May 20, 2022 (4 years ago)

Blue Moose Spinach Artichoke Parmesan Dip recall

Recalled by Blue Moose of Boulder, LLC · Lafayette, CO, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Spinach Artichoke Cashew Dip was mislabeled with Spinach Artichoke Parmesan Dip label and does not state that the product contains cashews and soy.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

Blue Moose Spinach Artichoke Parmesan Dip, 7 oz. (198g), packed in a square, clear plastic container, six units in a pack, UPC 8 47847 00467 5, Blue Moose of Boulder, LLC, 1733 Majestic Dr., Lafayette, CO 80026. Store under refrigeration 33 - 41 degrees F.

Quantity: 572 cases (6 units per case)

Food: Cheese Leafy greens & salads Sauces, dips & dressings

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 Code - SS446931 Best By - 08/10/2022

Where it was sold

California Ohio

FDA's distribution note: CA, OH. Note: Ohio product was destroyed upon customer receipt as firm had already determined the problem while enroute.

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. 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
Blue Moose of Boulder, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
May 20, 2022
In FDA report of
Jun 22, 2022
Terminated
Aug 25, 2022
FDA recall number
F-1306-2022 · event 90254
Official record
FDA enforcement report search

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