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Laird Superfood
Recall · Class III2019-05-24Terminated

The product is incorrectly labeled with 14 mg of Iron and 78% DV when the actual amount is 14 mcg of Iron and 0% DV.

Issued by the US Food and Drug Administration, naming Laird Superfood.

What the notice covered

Performance Mushrooms product is dried mushroom blend of 4 different mushroom mycelial biomass powders cultured on certified organic oats, brand Laird Superfood, uses as Beverage Booster and Functional Fuel Supplement. Product is packaged in 3.17 oz (90 gram) stand up with zipper, heat-sealed pouches. There are 6 pouches per case or 24 pouches cases.

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 III means

The FDA’s least serious class: use of the product is not likely to cause adverse health consequences. Often a labelling or packaging fault.

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-1456-2019
Kind of action
Recall
Dated
2019-05-24
Terminated
2019-10-23
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-1456-2019"

To see it in the FDA’s own words, search the reference number F-1456-2019 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