Member's Mark Super Greens Dietary Supplement; 48 servings; Net Weight 18.28 oz (518.4g) UPC: 193968490775
Summary
The FDA issued a Class I for Member's Mark Super Greens Dietary Supplement; 48 servings; Net Weight 18.28 oz by MeriCal, LLC. Reason: Potential contamination of Salmonella Richmond.
Details
Source
Food Recall
External ID
H-0205-2026
Action Date
2025-12-03
Status
Ongoing
Category
food
Product Description
Member's Mark Super Greens Dietary Supplement; 48 servings; Net Weight 18.28 oz (518.4g) UPC: 193968490775
Lot/Code Info: 500-00055034; 500-00055035; 500-00055036; 500-00055037; 500-00055038; 500-00055039 500-00055040; 500-00055042; 500-00055043; 500-00055044; 500-00055045; 500-00055046 500-00055047; 500-00055048; 500-00055049; 500-00055050; 500-00055051; 500-00055052 500-00055053; 500-00055054; 500-00055055; 500-00055056; 500-00055057; 500-00055058 500-00056121; 500-00056122; 500-00056123; 500-00056124; 500-00056125; 500-00056126 500-00056127; 500-00056128; 500-00056129; 500-00056130; 500-00056131; 500-00056132 500-00056133; 500-00056134; 500-00056135; 500-00056136; 500-00056137; 500-00056138 500-00056139; 500-00056140; 500-00056141; 500-00056142; 500-00056143; 500-00056144 500-00056145; 500-00056146; 500-00056147; 500-00056148; 500-00056149; 500-00056150 500-00056151; 500-00056152; 500-00056153; 500-00056154; 500-00056155; 500-00056230 500-00056231; 500-00056318; 500-00056323; 500-00056429; 500-00056772;
Quantity Affected: 698,064 units
Reason for Recall
Potential contamination of Salmonella Richmond
Distribution
Product was distributed to consignee locations across the country.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-24
Company
Anaheim, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 18 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (MeriCal, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does MeriCal, LLC have FDA actions?
This is the only FDA action we have on record for MeriCal, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0205-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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