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Stop using now Food recall · FDA · Published October 24, 2025

Member's Mark Super Greens Recalled for Salmonella Risk

MeriCal, LLC recalls Member's Mark Super Greens due to potential Salmonella Richmond contamination. Check your UPC and lot numbers immediately.

🇺🇸 FDA recall #H-0205-2026FoodMember's Mark ›
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Recalling firmMeriCal, LLC2995 E Miraloma Ave · Anaheim, CA 92806-1805
✎ GovInfoNow plain-language explainer

MeriCal, LLC is recalling Member's Mark Super Greens Dietary Supplement because it may be contaminated with Salmonella Richmond. The product was distributed nationwide to consignee locations. No remedy or return instructions are currently listed in the record. Read more at govinfonow.com/recall/7055-member-s-mark-super-greens-recalled-for-salmonella-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/7055-member-s-mark-super-greens-recalled-for-salmonella-risk · Updated October 9, 2026 · Official notice: FDA #H-0205-2026

Cite this page

“Member's Mark Super Greens Recalled for Salmonella Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/7055-member-s-mark-super-greens-recalled-for-salmonella-risk. Based on FDA recall #H-0205-2026.

The FDA announced on Oct. 24, 2025, that MeriCal, LLC is recalling Member's Mark Super Greens Dietary Supplement due to potential Salmonella Richmond contamination. Owners should stop using the product and contact the company for a refund.

How to tell if you have it

  • Member's Mark Super Greens Dietary Supplement
  • 48 servings
  • Net Weight 18.28 oz (518.4g)
  • UPC: 193968490775
  • Lot codes: 500-00055034 through 500-00055058, 500-00056121 through 500-00056155, 500-00056230, 500-00056231, 500-00056318, 500-00056323, 500-00056429, 500-00056772

The hazard

The product may be contaminated with Salmonella Richmond. The FDA classifies this as a Class I recall, the most serious category, indicating a reasonable probability that the product will cause serious adverse health consequences or death.

Context

GovInfoNow's records show MeriCal, LLC has issued three other recalls since March 19, 2019, including a Jan. 9, 2020, recall for missing shellfish allergen warnings and a Oct. 31, 2019, recall for an incorrect probiotic blend. Other recent recalls of similar products include Superfoods Live it Up Super Greens Recall (Jan. 15, 2026), Live it Up Super Greens Recall (Jan. 15, 2026), and Food to Live Organic Supergreens Powder Mix Recalled Due to Salmonella Contamination (Nov. 11, 2025).

How to tell if you have this one

Check your container for the UPC 193968490775 and any of the following lot numbers: 500-00055034 through 500-00055058, 500-00056121 through 500-00056155, 500-00056230, 500-00056318, 500-00056323, 500-00056429, or 500-00056772.

  • Brand
    Member's Mark
  • Product
    Member's Mark Super Greens Dietary Supplement; 48 servings; Net Weight 18.28 oz (518.4g) UPC: 193968490775
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the Member's Mark Super Greens Dietary Supplement if you have any of the identified lot numbers.

  2. Check your lot number

    Verify if your container matches UPC 193968490775 and one of the listed lot codes to confirm if it is part of this recall.

  3. Monitor for symptoms

    If you have consumed this product, watch for signs of Salmonella infection such as diarrhea, fever, or abdominal cramps.

Where it went and when

Where it was distributed

Distributed nationwide.

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: “Product was distributed to consignee locations across the country.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 40 days after the firm started it.

1. Firm started the recall: Oct 24, 202512. FDA classified it Class I: Nov 21, 202523. Published in FDA’s Enforcement Report: Dec 3, 202532025
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report

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 #H-0205-2026 (October 24, 2025)
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 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