World Organix Blissful Remedies Red Maeng Da Capsules Recall: Microbial Contamination Risk
World Organix recalls some Blissful Remedies Red Maeng Da capsules due to potential microbial contamination. Products with UPC#7 22589 32355 3 and Lot Code 102710 may be unsafe.
Recall notice
Microbial Contamination of Non-Sterile Products: The firm is initiating a recall of some of its products due to the potential of high microbial loads.
Contact the company
What happened, in plain English
World Organix is recalling certain Blissful Remedies Red Maeng Da capsules because they may contain high levels of microbes. This could pose a health risk if consumed. Read more at govinfonow.com/recall/40397-world-organix-blissful-remedies-red-maeng-da-capsules-recall-microbial.
Source Summary by GovInfoNow · govinfonow.com/recall/40397-world-organix-blissful-remedies-red-maeng-da-capsules-recall-microbial · Updated October 6, 2026 · FDA enforcement record: FDA #D-1122-2018
Cite this page
“World Organix Blissful Remedies Red Maeng Da Capsules Recall: Microbial Contamination Risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/40397-world-organix-blissful-remedies-red-maeng-da-capsules-recall-microbial. Based on FDA recall #D-1122-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1122-2018%22&limit=1).
Why it’s dangerous
The capsules may have high microbial loads, which can lead to health issues if consumed. This contamination risk is specific to non-sterile products that are intended for consumption.
Who’s affected
Anyone who owns or uses the recalled Blissful Remedies Red Maeng Da capsules with UPC#7 22589 32355 3 and Lot Code 102710. People who consume these capsules are at risk of potential microbial contamination.
How to tell if you have this one
Check for the UPC#7 22589 32355 3 and Lot Code 102710 on the packaging. The product is a 50-count White Foil Pouche of Blissful Remedies Red Maeng Da capsules.
- Brand
World Organix- Product
Blissful Remedies Red Maeng Da, 100% Mitragyna Speciosa capsule, 50-count packaged White Foil Pouche, Dist. by World- Category
Drug
All 5 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
Nationwide in the USA.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-1122-2018 | Blissful Remedies Red Maeng Da, 100% Mitragyna Speciosa capsule, 50-count packaged White Foil Pouche, Dist. by World Organix LLC, Las Vegas, Nevada UPC#7 22589 32355 3; Lot Code: 102710. Best by date: 03/2019 | 789 50-count pouches, total of 39,450 capsules |
| D-1123-2018 | Blissful Remedies, 4 Hour Chill, Slow Motion Blend, Herbal Shot. 1.93 Fluid Oz (57ml) UPC#6 02401 88900 3.; Lot Code: 22. Best by date: 06/2019 | 164 2oz bottles |
| D-1124-2018 | Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa, 12mL bottle. Distributed by World Organix LLC Las Vegas Nevada. UPC#7 14983 56525 7; Lot Code: 2001. Best by date: 03/2019 | 681 12 mL-bottle |
| D-1125-2018 | Blissful Remedies Gold Series Ultra Enhanced Indo, 50 capsule, packaged in While Foil Pouch, Dist. by World Organix LLC, Las Vegas Nevada UPC# 6 02401 88900 2; Lot Code: 112710 Exp 03/2019 | 545 50-count pouches, 27,250 capsules |
| D-1126-2018 | Blissful Remedies Kratom+CBD CBD infused Maeng Da, capsules 50-count packaged in While Foil Pouch. Dist. by World Organix LLC, Las Vegas Nevada UPC# 7 11583 27057 4; Lot Code: 112710 Exp 03/2019 | 553 50-count pouch, 27,650 capsules |
What to do — step by step
Check Product Details
Look for the UPC#7 22589 32355 3 and Lot Code 102710 on the packaging to confirm if the product is recalled.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide in the USA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 6.3 years after the firm started it.
- Firm started the recall
- Published in FDA’s Enforcement Report
- FDA classified it Class I
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
When was this product sold?
The product was sold with a best by date of 03/2019.
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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 #D-1122-2018 (June 26, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1122-2018 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.