Class ITerminated in FDA datasetRecall initiated Mar 9, 2018

NXTGEN Botanicals, Maeng Da Kratom, Dietary Supplement, 70 Capsules, Made in the U.S.A

Recalling firm: Avalon Packaging

Why it was recalled

Avalon Packaging is recalling NXTGEN Kratom because of the potential for Salmonella contamination.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 22, 2020.

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ProductNXTGEN Botanicals, Maeng Da Kratom, Dietary Supplement, 70 Capsules, Made in the U.S.A

FDA code information

Lot 171409

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Full FDA record and distribution details

Original product description

NXTGEN Botanicals, Maeng Da Kratom, Dietary Supplement, 70 Capsules, Made in the U.S.A

Original FDA recall reason

Avalon Packaging is recalling NXTGEN Kratom because of the potential for Salmonella contamination.

Recall details

Recall number
F-0996-2018
Event ID
79477
FDA status
Terminated
Initiated
Mar 9, 2018
Reported
Mar 28, 2018
Classified
Apr 4, 2018
Terminated
Jan 22, 2020
Quantity
1108 bottles
Location
Orem, UT, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

Sold to Label owner in UT.

FDA source record · F-0996-2018

Data updated September 16, 2026. View official FDA data ↗

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