Toxin Absorber with Organic Peppermint Leaf - 14 packets and 30 packets
Recalling firm: NUTRANEXT BUSINESS LLC
Routine quality testing identified elevated levels of lead above applicable 2232 levels, which may pose potential health risks to a portion of the population.
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: Jul 2, 2019.
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FDA code information
14 Packets: Batch: 1078290, 1049756, 1037001, 1032699. 30 Packets: Batch: 1085169, 1081135, 1066646, 1053751, 1049757, 1042085, 1040682, 1036938, 1032700.
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Full FDA record and distribution details
Original product description
Toxin Absorber with Organic Peppermint Leaf - 14 packets and 30 packets
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| batch | 1036938 | Packets: Batch: 1085169, 1081135, 1066646, 1053751, 1049757, 1042085, 1040682, 1036938, 1032700. |
| batch | 1040682 | 2699. 30 Packets: Batch: 1085169, 1081135, 1066646, 1053751, 1049757, 1042085, 1040682, 1036938, 1032700. |
| batch | 1042085 | 7001, 1032699. 30 Packets: Batch: 1085169, 1081135, 1066646, 1053751, 1049757, 1042085, 1040682, 1036938, 1032700. |
| batch | 1049757 | 9756, 1037001, 1032699. 30 Packets: Batch: 1085169, 1081135, 1066646, 1053751, 1049757, 1042085, 1040682, 1036938, 1032700. |
| batch | 1053751 | 8290, 1049756, 1037001, 1032699. 30 Packets: Batch: 1085169, 1081135, 1066646, 1053751, 1049757, 1042085, 1040682, 1036938, 1032700. |
| batch | 1066646 | atch: 1078290, 1049756, 1037001, 1032699. 30 Packets: Batch: 1085169, 1081135, 1066646, 1053751, 1049757, 1042085, 1040682, 1036938, 1032700. |
| batch | 1081135 | ackets: Batch: 1078290, 1049756, 1037001, 1032699. 30 Packets: Batch: 1085169, 1081135, 1066646, 1053751, 1049757, 1042085, 1040682, 1036938, 1032700. |
| batch | 1085169 | 14 Packets: Batch: 1078290, 1049756, 1037001, 1032699. 30 Packets: Batch: 1085169, 1081135, 1066646, 1053751, 1049757, 1042085, 1040682, 1036938, 1032700. |
Original FDA recall reason
Routine quality testing identified elevated levels of lead above applicable 2232 levels, which may pose potential health risks to a portion of the population.
Recall details
- Recall number
- F-0409-2019
- Event ID
- 81215
- FDA status
- Terminated
- Initiated
- Oct 1, 2018
- Reported
- Nov 14, 2018
- Classified
- Nov 8, 2018
- Terminated
- Jul 2, 2019
- Quantity
- 1,986 units (1,734 - 30 packets) (252 - 14 packets)
- Location
- Sunrise, FL, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
Where it was distributed
US and Foreign Consignees only. No government consignees.
Data updated September 16, 2026. View official FDA data ↗
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