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NGB, Corp Recall: NGB Corp is recalling Nxtgen Botanicals due to potential Salmonella contamination. - F-1134-2018

United States

TerminatedClass I

Company
NGB, Corp
Product
Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 c…
Recall date
March 16, 2018
Terminated
January 22, 2020
Source
FDA

Reason for recall

NGB Corp is recalling Nxtgen Botanicals due to potential Salmonella contamination.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 capsules Not published in this source record 12,450 Bottles Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424

Distribution

  • Retailers nationwide. No military/govt/VA/foreign consignees.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1134-2018
Event ID
79794
Status
Terminated
Classification
Class I
Company
NGB, Corp
Product description
Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 capsules
Quantity
12,450 Bottles
Reason
NGB Corp is recalling Nxtgen Botanicals due to potential Salmonella contamination.
Recall initiation date
March 16, 2018
Report date
May 2, 2018
Classification date
Not published in this source record
Termination date
January 22, 2020
Distribution pattern
Retailers nationwide. No military/govt/VA/foreign consignees.
UPC, lot, and code information
Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: NGB, Corp

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Virginia 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of January 22, 2020.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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