Severity
Critical
CriticalClass ITerminated
FDA Food recall · Reported April 25, 2018
Nirvanio Maeng Da Kratom all packages, all quantities
Dietary supplements have the potential to be contaminated with Salmonella.
The recall
Nutrizone LLC issued this critical-severity FDA Food recall — Dietary supplements have the potential to be contaminated with Salmonella..
- Critical
- severity level
- Class I
- classification
- April 25, 2018
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1384-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1384-2018) was formally reported on April 25, 2018, with the manufacturer initiating the action on March 30, 2018. It is classified under Critical severity (Class I), with a current status of Terminated. Nutrizone LLC is listed as the recalling firm, operating out of Houston, TX. Federal records list the affected scope as Approximately 5517 units.
The documented reason for this recall is: Dietary supplements have the potential to be contaminated with Salmonella. Distribution data in the federal record shows the product reached: Nationwide (FL, CA,OK,GA,SC,PA,LA,WA,MS,MO,KY,AZ,CO,TX, NY,IL). 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 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 — 711 dietary supplements recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified high severity.
Affected scope
Approximately 5517 units
Related Recalls
6
5 from same agency
Product description
Nirvanio Maeng Da Kratom all packages, all quantities
Reason for recall
Dietary supplements have the potential to be contaminated with Salmonella.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-1384-2018 |
| Date reported | April 25, 2018 |
| Date initiated | March 30, 2018 |
| Recalling firm | Nutrizone LLC |
| Firm location | Houston, TX |
| Affected scope | Approximately 5517 units |
| Distribution | Nationwide (FL, CA,OK,GA,SC,PA,LA,WA,MS,MO,KY,AZ,CO,TX, NY,IL) |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
Frequently Asked Questions
What product was recalled? ▼
Nirvanio Maeng Da Kratom all packages, all quantities. Recalled by Nutrizone LLC. Units affected: Approximately 5517 units.
Why was this product recalled? ▼
Dietary supplements have the potential to be contaminated with Salmonella.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on April 25, 2018. Severity: Critical. Recall number: F-1384-2018.
Where was the recalled product distributed? ▼
Distribution: Nationwide (FL, CA,OK,GA,SC,PA,LA,WA,MS,MO,KY,AZ,CO,TX, NY,IL).
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1384-2018) 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.
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported April 25, 2018.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
Source: Federal recall agencies (FDA, CPSC, NHTSA) Aggregated federal recall feeds Recall data normalized across FDA, CPSC and NHTSA feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type).