Nutranext Business Internal Cleansing Kit Peppermint Recall

Why it was recalled

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

Product description

Internal Cleansing Kit Peppermint

Lot numbers, UPCs & expiration codes

Batch # SC69 SC69 SC68 SC69 SC68 SC68 SC65 SC66 SC65 SC65 SC629 SC613 SC607 SC587 SC583 SC576 SC566 SC560 SC556 SC543 SC532 SC527 SC519 SC507

Where it was sold

US and Foreign Consignees only. No government consignees.

What to do if you have this product

Compare the brand, size, and lot/UPC codes on your package with the codes above.
If it matches, don't eat it. Return it to the store for a refund or throw it away.
Wash surfaces and containers that touched the product.
If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number: F-0412-2019
Classification: Class II
Status: Terminated
Recall initiated: Oct 1, 2018
FDA report date: Nov 14, 2018
Quantity: 2387 pkgs
Recall type: Voluntary: Firm initiated
Recalling firm: NUTRANEXT BUSINESS LLC

Original FDA data

Every field from FDA enforcement report F-0412-2019, exactly as published.

Show all FDA fields

City: Sunrise
State: FL
Status: Terminated
Country: United States
Event ID: 81215
Address: 1301 Swgrs Corp Pkwy
Code information: Batch # SC69 SC69 SC68 SC69 SC68 SC68 SC65 SC66 SC65 SC65 SC629 SC613 SC607 SC587 SC583 SC576 SC566 SC560 SC556 SC543 SC532 SC527 SC519 SC507
Postal code: 33323-2813
Report date: Nov 14, 2018
Product type: Food
Recall number: F-0412-2019
Classification: Class II
Recalling firm: NUTRANEXT BUSINESS LLC
Product quantity: 2387 pkgs
Termination date: Jul 2, 2019
Reason for recall: Routine quality testing identified elevated levels of lead above applicable 2232 levels, which may pose potential health risks to a portion of the population.
Voluntary / mandated: Voluntary: Firm initiated
Product description: Internal Cleansing Kit Peppermint
Distribution pattern: US and Foreign Consignees only. No government consignees.
Recall initiation date: Oct 1, 2018
Initial firm notification: E-Mail
Center classification date: Nov 8, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0412-2019, published Nov 14, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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