Blue Moose Spinach Artichoke Parmesan Dip, 7 oz. (198g), packed in a square, clear plastic container, six units in a pac
Summary
The FDA issued a Class I for Blue Moose Spinach Artichoke Parmesan Dip, 7 oz. (198g), packed in a square, cle by Blue Moose of Boulder, LLC. Reason: Spinach Artichoke Cashew Dip was mislabeled with Spinach Artichoke Parmesan Dip label and does not state that the product contains cashews and soy..
Details
Source
Food Recall
External ID
F-1306-2022
Action Date
2022-06-22
Status
Terminated
Category
food
Product Description
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.
Lot/Code Info: Lot Code - SS446931 Best By - 08/10/2022
Quantity Affected: 572 cases (6 units per case)
Reason for Recall
Spinach Artichoke Cashew Dip was mislabeled with Spinach Artichoke Parmesan Dip label and does not state that the product contains cashews and soy.
Distribution
CA, OH. Note: Ohio product was destroyed upon customer receipt as firm had already determined the problem while enroute.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-20
Company
Lafayette, CO
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 175 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Blue Moose of Boulder, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Blue Moose of Boulder, LLC have FDA actions?
This is the only FDA action we have on record for Blue Moose of Boulder, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1306-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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