Severity
Critical
CriticalClass ITerminated
FDA Food recall · Reported October 3, 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.
The firm distributes dietary supplements which contain Mitragyna speciosa (kratom) a dietary ingredient with inadequate information to provide reasonable assurance that such ingre…
Zakah Life LLC recalled Super Green Maeng Da Premium Kratom, Zakah Life Dietary Supplement, Mitragyn Speciosa, pa… - a critical-severity action.
Super Green Maeng Da Premium Kratom, Zakah Life Dietary Supplement, Mitragyn Speciosa, pa… was recalled by Zakah Life LLC in October 3, 2018. Reason: The firm distributes dietary supplements which contain Mitragyna speciosa (kratom) a dietary ingredient with …. Check the official notice for the remedy. Verify recall #F-1983-2018 with the FDA Food before acting.
The recall
Zakah Life LLC issued this critical-severity FDA Food recall-The firm distributes dietary supplements which contain Mitragyna speciosa (kratom) a dietary ingredient with ….
- Critical
- severity level
- Class I
- classification
- October 3, 2018
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1983-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1983-2018) was formally reported on October 3, 2018, with the manufacturer initiating the action on August 3, 2018. It is classified under Critical severity (Class I), with a current status of Terminated. Zakah Life LLC is listed as the recalling firm, operating out of Ankeny, IA. Federal records list the affected scope as 46 100g bags and 12 bottles and 8.4 kg of capsules..
The documented reason for this recall is: 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 … Distribution data in the federal record shows the product reached: Distributed to consumers and retailers in Colorado, Illinois, Iowa, and Nebraska. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
46 100g bags and 12 bottles and 8.4 kg of capsules.
Related Recalls
6
6 from same agency
Product description
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.
Reason for 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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-1983-2018 |
| Date reported | October 3, 2018 |
| Date initiated | August 3, 2018 |
| Recalling firm | Zakah Life LLC |
| Firm location | Ankeny, IA |
| Affected scope | 46 100g bags and 12 bottles and 8.4 kg of capsules. |
| Distribution | Distributed to consumers and retailers in Colorado, Illinois, Iowa, and Nebraska |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-1983-2018) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Zakah Life LLC. Units affected: 46 100g bags and 12 bottles and 8.4 kg of capsules..
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on October 3, 2018. Severity: Critical. Recall number: F-1983-2018.
Where was the recalled product distributed? ▼
Distribution: Distributed to consumers and retailers in Colorado, Illinois, Iowa, and Nebraska.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1983-2018) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported October 3, 2018. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.