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Lower risk Food recall · FDA · Published May 24, 2019

Laird Superfood Performance Mushrooms Recall: Iron Labeling Error

Laird Superfood recalls Performance Mushrooms due to incorrect iron labeling. The product claims 14 mg of iron, but contains only 14 mcg.

🇺🇸 FDA recall #F-1456-2019FoodLaird Superfood ›
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Recalling firmLAIRD SUPERFOOD INC295 W Lundgren Mill Dr · Sisters, OR 97759
✎ GovInfoNow plain-language explainer

Laird Superfood Inc. is recalling its Performance Mushrooms product because the label incorrectly states it contains 14 mg of Iron and 78% Daily Value. In reality, the product contains only 14 mcg of Iron and 0% Daily Value. This is a Class III recall involving an estimated 24,862 pouches distributed nationwide and in Canada. Read more at govinfonow.com/recall/17418-laird-superfood-performance-mushrooms-recall-iron-labeling-error.

Source Summary by GovInfoNow · govinfonow.com/recall/17418-laird-superfood-performance-mushrooms-recall-iron-labeling-error · Updated October 11, 2026 · FDA enforcement record: FDA #F-1456-2019

Cite this page

“Laird Superfood Performance Mushrooms Recall: Iron Labeling Error.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/17418-laird-superfood-performance-mushrooms-recall-iron-labeling-error. Based on FDA recall #F-1456-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1456-2019%22&limit=1).

The FDA announced on May 24, 2019, that Laird Superfood is recalling Performance Mushrooms Supplement due to incorrect iron labeling. The product lists 14 mg of iron when it actually contains 14 mcg.

How to tell if you have it

  • Brand: Laird Superfood
  • Product: Performance Mushrooms Supplement
  • Lot numbers: 2401192904, B000975-3.5-0711, B000975-3.5-0712, B001010-3.5-0208, B001010-3.5-0211, B001010-3.5-0212, B000979-2L-0927, B000979-2L-0928
  • Best By dates: 10/2020, 12/2020, 06/2021

The hazard

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.

Context

GovInfoNow's records show other recent recalls of similar products include Prospector Popcorn Belgian Chocolate Toffee Gourmet Popcorn Recall (2026-07-15), Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn Recall (2026-07-15), and Prospector Popcorn Recall (2026-07-15).

How to tell if you have this one

Check for the brand Laird Superfood and product name Performance Mushrooms in a 3.17 oz (90 gram) stand-up pouch with a zipper. Look for these specific lot numbers: 2401192904, B000975-3.5-0711, B000975-3.5-0712, B001010-3.5-0208, B001010-3.5-0211, B001010-3.5-0212, B000979-2L-0927, and B000979-2L-0928. Verify the Best By dates are 10/2020, 12/2020, or 06/2021.

  • Brand
    Laird Superfood
  • Category
    Food

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “distributed nationwide and in Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 5 months after the firm started it.

1. Firm started the recall: May 24, 201912. FDA classified it Class III: Jun 12, 201923. Published in FDA’s Enforcement Report: Jun 19, 201934. FDA terminated the recall: Oct 23, 201942019
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1456-2019 (May 24, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1456-2019 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA