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Blue Moose Of Boulder Llc
Recall · Class I2022-05-20Terminated

The label was wrong about what is inside.

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

Above, in the agency’s own words. The line before it is our plain-English summary — how we word these.

Issued by the US Food and Drug Administration, naming Blue Moose Of Boulder Llc.

What the notice covered

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.

Quoted from the record as published. If a product is not described here, this notice does not tell us whether it was affected.

What Class I means

The FDA’s most serious class: a reasonable probability that using the product will cause serious health consequences or death.

This is the agency’s own definition of the class. We do not assign classes and we do not rank them against each other.

The record

Agency
US Food and Drug Administration (FDA)
Reference number
F-1306-2022
Kind of action
Recall
Dated
2022-05-20
Terminated
2022-08-25
Status on the record
Terminated
We read it
2026-10-01

Regulates most packaged food, drugs and devices. Its recall records are published weekly in the Enforcement Report.

Products we matched to this notice

We have not matched this notice to any product in our database — usually because it named no barcode we hold. Products may still have been affected.

How we are treating it

This notice concerns the product line itself or how it was produced.

The government record

The FDA publishes this notice through its enforcement API, so the link below returns raw JSON rather than a readable page. It is the primary record and we cite it as such; everything above is our transcription of it.

https://api.fda.gov/food/enforcement.json?search=recall_number:"F-1306-2022"

To see it in the FDA’s own words, search the reference number F-1306-2022 in the Search the FDA Enforcement Report. The FDA publishes no direct link to an individual recall.

How we source every record on this site