Recall Register

Food recall: Toxin Absorber with Organic Ginger Root - 14 packets and 30 packets

Class II FDA enforcement event 81215. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

Routine quality testing identified elevated levels of lead above applicable 2232 levels, which may pose potential health risks to a portion of the population.

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

NUTRANEXT BUSINESS LLC started this food recall on 1 Oct 2018. The firm address in the FDA record is in Sunrise, FL. FDA put the recall in Class II. FDA event 81215 has 8 product records. The first FDA enforcement report date is 14 Nov 2018. The record gives the status Terminated, with the termination date 2 Jul 2019.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

US and Foreign Consignees only. No government consignees.

Recalling firm

NUTRANEXT BUSINESS LLC, Sunrise, FL.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

8 product records in the event.

FDA event 81215: product records
Recall numberProductQuantityClassStatusReport date
F-0408-2019Toxin Absorber with Organic Ginger Root - 14 packets and 30 packets5,456 units (4,515 - 30 packets) (941 - 14 packets)Class IITerminated14 Nov 2018
F-0409-2019Toxin Absorber with Organic Peppermint Leaf - 14 packets and 30 packets1,986 units (1,734 - 30 packets) (252 - 14 packets)Class IITerminated14 Nov 2018
F-0410-2019Colon Cleansing Kit Ginger17,625 pkgsClass IITerminated14 Nov 2018
F-0411-2019Colon Cleansing Kit Peppermint7638 pkgsClass IITerminated14 Nov 2018
F-0412-2019Internal Cleansing Kit Peppermint2387 pkgsClass IITerminated14 Nov 2018
F-0413-2019Internal Cleansing Kit Ginger6144 pkgsClass IITerminated14 Nov 2018
F-0414-2019Parasite Cleansing Kit Ginger2472 pkgsClass IITerminated14 Nov 2018
F-0415-2019Parasite Cleansing Kit Peppermint839 pkgsClass IITerminated14 Nov 2018

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Food events that started in 2018
578
Share of these events in Class II
56%
Product records in this event
8
Events of the firm on the register
1

Official channels

Cite this page

Recall Register. FDA enforcement event 81215. https://recallregister.com/fda/ii/81215/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA food enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: US and Foreign Consignees only. No government consignees.
What quantity of product is in FDA event 81215?
The event has 8 product records. The first record gives this quantity: 5,456 units (4,515 - 30 packets) (941 - 14 packets)
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many food recalls of 2018 have the same class?
56% of the 578 food events that started in 2018 are in Class II.