Club 13 Kratom Capsules Recall: Salmonella Risk in Some Products
Club 13 Enterprises Warehouse recalls Kratom capsules due to Salmonella contamination in samples. Affected products include 5, 20, 25, 40, and 50-count bottles with specific lot numbers.
Lower-risk recall
Samples of Maeng Da red powder were tested and resulted positive for Salmonella.
Contact the company
What happened, in plain English
Club 13 Enterprises Warehouse is recalling Kratom Maeng Da Red XS capsules because samples tested positive for Salmonella bacteria. This poses a risk of food poisoning if consumed, so affected consumers should stop using the products. Read more at govinfonow.com/recall/19270-club-13-kratom-capsules-recall-salmonella-risk-in-some-products.
Source Summary by GovInfoNow · govinfonow.com/recall/19270-club-13-kratom-capsules-recall-salmonella-risk-in-some-products · Updated October 7, 2026 · FDA enforcement record: FDA #F-1121-2018
Cite this page
“Club 13 Kratom Capsules Recall: Salmonella Risk in Some Products.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19270-club-13-kratom-capsules-recall-salmonella-risk-in-some-products. Based on FDA recall #F-1121-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1121-2018%22&limit=1).
Why it’s dangerous
Salmonella bacteria can cause food poisoning, leading to symptoms like diarrhea, fever, and stomach cramps. The contamination was detected in samples of the Kratom capsules, indicating potential health risks if ingested.
Who’s affected
Consumers who purchased Club 13 Kratom Maeng Da Red XS capsules in 5, 20, 25, 40, or 50-count bottles with lot numbers KRXS020718 through KRXS120117 are affected. Those who have consumed the product may face food poisoning risks.
How to tell if you have this one
Check for the product name 'Club 13 Kratom Maeng Da Red XS capsules' in 5, 20, 25, 40, or 50-count bottles. Look for lot numbers KRXS020718, KRXS030618, KRXS102417, KRXS110617, or KRXS120117 on the packaging.
- Brand
Club 13- 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.
- Classification
Class I- Status
Terminated- Distribution
U.S. consignees only.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-1119-2018 | Club 13 Kratom Maeng Da Red powder; Pouches of 15, 30, 90, 150, 454 grams, and Club 13 Kratom Maeng Da Red powder in bulk bags.; Lot # MRMD012618 | 10,237 units and 48 kg of bulk bags |
| F-1120-2018 | Club 13 Kratom Maeng Da Red capsules; 5, 25, 50, 100, 120 capsule bottles, and Club 13 Kratom Maeng Da Red capsules in bulk bags.; Lots # MRMD013018, MRMD013118, MRMD020118, MRMD020518, MRMD022318, MRMD022718, MRMD030118, MRMD030218, and MRMD030618. | 7,683 units and 128 kg of capsules in bulk bags |
| F-1121-2018 | Club 13 Kratom Maeng Da Red XS capsules; 5, 20, 25, 40, 50 capsule bottles; Lots # KRXS020718, KRXS030618, KRXS102417, KRXS110617, and KRXS120117. | 873 units |
What to do — step by step
Check Product Lot Number
Look for lot numbers KRXS020718, KRXS030618, KRXS102417, KRXS110617, or KRXS120117 on the capsule bottles.
How this recall unfolded
Recall timeline
FDA terminated this recall 12 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.
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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-1121-2018 (March 31, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1121-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.