Zakah Life Super Green Maeng Da Kratom Recall: Salmonella Risk
Zakah Life recalls Super Green Maeng Da Premium Kratom due to potential Salmonella contamination in red and green strains. The product may cause illness if consumed. Consumers should check labels for 90-capsule or 100g bags.
Lower-risk recall
The firm distributes dietary supplements which contain Mitragyna speciosa (kratom) a dietary ingredient with inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury. Also, based on FDA sample positive sample results, the red and green strains are potentially contaminated with Salmonella.
Contact the company
What happened, in plain English
Zakah Life is recalling Super Green Maeng Da Premium Kratom products because they may be contaminated with Salmonella, a bacteria that can cause food poisoning. This recall is due to FDA test results showing positive samples for Salmonella in the red and green strains of the product. Read more at govinfonow.com/recall/18769-zakah-life-super-green-maeng-da-kratom-recall-salmonella-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/18769-zakah-life-super-green-maeng-da-kratom-recall-salmonella-risk · Updated October 6, 2026 · FDA enforcement record: FDA #F-1983-2018
Cite this page
“Zakah Life Super Green Maeng Da Kratom Recall: Salmonella Risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18769-zakah-life-super-green-maeng-da-kratom-recall-salmonella-risk. Based on FDA recall #F-1983-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1983-2018%22&limit=1).
Why it’s dangerous
The product may contain Salmonella bacteria, which can cause food poisoning symptoms like diarrhea, fever, and stomach cramps. FDA testing found positive samples for Salmonella in the red and green strains of this Kratom product.
Who’s affected
People who own or use Zakah Life's Super Green Maeng Da Premium Kratom products, especially those who consume the red or green strains. Those with weakened immune systems may be at higher risk of illness.
How to tell if you have this one
Check for products labeled 'Super Green Maeng Da Premium Kratom' in 90-capsule bottles (500 mg per capsule) or 100g bags. The expiration date on the label is 06/2023.
- Brand
Zakah Life- Category
Food
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Status
Terminated- Distribution
Distributed to consumers and retailers in Colorado, Illinois, Iowa, and Nebraska
| Recall number | Product, codes & lots | Quantity | Class |
|---|---|---|---|
| F-1982-2018 | Powerful Red Vein Bali Premium Kratom, Zakah Life Dietary Supplement, Mitragyn Speciosa, packaged in 1) 90 capsules, 500 mg per capsules bottles, or 2) 3.52 oz // 100 grams of Kratom bags. Distributed by Zakah Life LLC Ankeny IA.; SG010118, Exp: 06/2023 | 30 100g bags and 12 bottles and 8.4 kg of capsules | Class I |
| F-1983-2018 | Super Green Maeng Da Premium Kratom, Zakah Life Dietary Supplement, Mitragyn Speciosa, packaged in 1) 90 capsules, 500 mg per capsules bottles, or 2) 3.52 oz // 100 grams of Kratom bags. Distributed by Zakah Life LLC Ankeny IA.; SG50118, Exp: 06/2023 | 46 100g bags and 12 bottles and 8.4 kg of capsules. | Class I |
| F-1984-2018 | Top Shelf White Maeng Da Premium Kratom, Zakah Life Dietary Supplement, Mitragyn Speciosa, packaged in 1) 90 capsules, 500 mg per capsules bottles, or 2) 3.52 oz // 100 grams of Kratom bags. Distributed by Zakah Life LLC Ankeny IA.; TS050118, Exp: 06/2023 | 10 100g bags | Class II |
What to do — step by step
Check Product Labels
Look for the product name and expiration date on the label to confirm if it's part of the recall.
Where it went and when
Where it was distributed
Distributed in 4 states.
FDA distribution: “Distributed to consumers and retailers in Colorado, Illinois, Iowa, and Nebraska” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Colorado, Illinois, Iowa, Nebraska.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Is this product safe to use?
The product may contain Salmonella, which can cause food poisoning. It is recommended to stop using the product until the recall is resolved.
Similar recalls
Latest food recalls
Keep exploring
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-1983-2018 (August 3, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1983-2018 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.