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Blue Moose of Boulder, LLC Recall: Spinach Artichoke Cashew Dip was mislabeled with Spinach Artichoke Parmesan Dip label and does not state that the product contains cashews and soy.

United States

TerminatedClass I

Company
Blue Moose of Boulder, LLC
Product
Blue Moose Spinach Artichoke Parmesan Dip, 7 oz. (198g), pac…
Recall date
May 20, 2022
Terminated
August 25, 2022
Source
FDA

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.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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. Not published in this source record 572 cases (6 units per case) Lot Code - SS446931 Best By - 08/10/2022

Distribution

  • CA
  • OH. Note: Ohio product was destroyed upon customer receipt as firm had already determined the problem while enroute.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1306-2022
Event ID
90254
Status
Terminated
Classification
Class I
Company
Blue Moose of Boulder, LLC
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.
Quantity
572 cases (6 units per case)
Reason
Spinach Artichoke Cashew Dip was mislabeled with Spinach Artichoke Parmesan Dip label and does not state that the product contains cashews and soy.
Recall initiation date
May 20, 2022
Report date
June 22, 2022
Classification date
Not published in this source record
Termination date
August 25, 2022
Distribution pattern
CA, OH. Note: Ohio product was destroyed upon customer receipt as firm had already determined the problem while enroute.
UPC, lot, and code information
Lot Code - SS446931 Best By - 08/10/2022
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Blue Moose of Boulder, LLC

Other recalls from Blue Moose of Boulder, LLC

FDA Recall United States Terminated Historical recordClass I

Blue Moose of Boulder, LLC

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Published
March 21, 2018
Distribution
Colorado, Utah, Kansas. No foreign/VA/g…

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Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
California 1
Ohio 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

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