Severity
Critical
CriticalClass ITerminated
FDA Drug recall · Reported August 15, 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
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.
World Organix, LLC recalled Blissful Remedies Red Maeng Da, 100% Mitragyna Speciosa capsule, 50-count packaged White … - a critical-severity action.
Blissful Remedies Red Maeng Da, 100% Mitragyna Speciosa capsule, 50-count packaged White … was recalled by World Organix, LLC in August 15, 2018. Reason: Microbial Contamination of Non-Sterile Products: The firm is initiating a recall of some of its products due …. Check the official notice for the remedy. Verify recall #D-1122-2018 with the FDA Drug before acting.
The recall
World Organix, LLC issued this critical-severity FDA Drug recall-Microbial Contamination of Non-Sterile Products: The firm is initiating a recall of some of its products due ….
- Critical
- severity level
- Class I
- classification
- August 15, 2018
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-1122-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-1122-2018) was formally reported on August 15, 2018, with the manufacturer initiating the action on June 26, 2018. It is classified under Critical severity (Class I), with a current status of Terminated. World Organix, LLC is listed as the recalling firm, operating out of Las Vegas, NV. Federal records list the affected scope as 789 50-count pouches, total of 39,450 capsules.
The documented reason for this recall is: 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. Distribution data in the federal record shows the product reached: Nationwide in the USA.. 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, 5 from FDA Drug - 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.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications 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
789 50-count pouches, total of 39,450 capsules
Related Recalls
6
5 from same agency
Product description
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
Reason for recall
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | D-1122-2018 |
| Date reported | August 15, 2018 |
| Date initiated | June 26, 2018 |
| Recalling firm | World Organix, LLC |
| Firm location | Las Vegas, NV |
| Affected scope | 789 50-count pouches, total of 39,450 capsules |
| Distribution | Nationwide in the USA. |
Profile values are sourced directly from the official FDA Drug 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 (D-1122-2018) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug 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 Drug 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? ▼
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. Recalled by World Organix, LLC. Units affected: 789 50-count pouches, total of 39,450 capsules.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 15, 2018. Severity: Critical. Recall number: D-1122-2018.
Where was the recalled product distributed? ▼
Distribution: Nationwide in the USA..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-1122-2018) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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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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 Drug, reported August 15, 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.