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Use caution Food recall · FDA · Published July 6, 2018

Earthrise Natural Spirulina Recall: Small Metal Pieces Hazard

Earthrise Nutritionals recalls 20kg spirulina with possible small metal pieces from sifter screens. Check lot numbers 17950-17983 and use by dates 8/22/2021 to 9/3/2021.

🇺🇸 FDA recall #F-1620-2018FoodEarthrise ›
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Contact the company

Recalling firmEarthrise Nutritionals Llc2151 Michelson Dr Ste 258 · Irvine, CA 92612-1382
✎ GovInfoNow plain-language explainer

What happened, in plain English

Earthrise Nutritionals is recalling 20kg natural spirulina products that may contain small metal pieces from sifter screens. This could cause injury if swallowed, so affected consumers should stop using the product. Read more at govinfonow.com/recall/19004-earthrise-natural-spirulina-recall-small-metal-pieces-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/19004-earthrise-natural-spirulina-recall-small-metal-pieces-hazard · Updated October 6, 2026 · FDA enforcement record: FDA #F-1620-2018

Cite this page

“Earthrise Natural Spirulina Recall: Small Metal Pieces Hazard.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/19004-earthrise-natural-spirulina-recall-small-metal-pieces-hazard. Based on FDA recall #F-1620-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1620-2018%22&limit=1).

Why it’s dangerous

The spirulina product may contain small metal pieces (2-8 mm) from a sifter screen during manufacturing. If swallowed, these metal pieces could cause injury to the mouth, throat, or digestive system.

Who’s affected

People who purchased Earthrise Natural Spirulina with lot numbers 17950 to 17983 between August 22 and September 3, 2021. Those who consume the product are at risk of injury from swallowing metal pieces.

How to tell if you have this one

Check the product label for lot numbers 17950 to 17983 and use by dates from August 22 to September 3, 2021. The product comes in double-sealed bags with a net weight of 20 kg (44 lbs).

  • Brand
    Earthrise
  • Product
    Earthrise Natural Spirulina; Net Weight: 20.0 kg( 44.0 lbs); Double bag sealed - 1 bag per box. UPC: 0 32602 99040 3
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for lot numbers 17950 to 17983 and use by dates from August 22 to September 3, 2021.

  2. Stop Using Product

    If you have the recalled product, stop using it immediately to avoid potential injury from swallowed metal pieces.

Where it went and when

Where it was distributed

Distributed in 10 states, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: yesUTColorado: not listedCONebraska: not listedNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: yesHITexas: yesTXFlorida: not listedFL

FDA distribution: “CA, AZ, UT, HI, OR. WA, MO, NY, TX, IL, and Aruba, Canada, Germany,” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, Hawaii, Illinois, Missouri, New York, Oregon, Texas, Utah, Washington.

Recall timeline

FDA terminated this recall 9 months after the firm started it.

1. Firm started the recall: Jul 6, 201812. FDA classified it Class II: Jul 12, 201823. Published in FDA’s Enforcement Report: Jul 18, 201834. FDA terminated the recall: Apr 19, 2019420182019
  1. Firm started the recall
  2. FDA classified it Class II
  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-1620-2018 (July 6, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1620-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 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