FDA Recall United States Ongoing Historical recordClass I
Pious Lion
- Product
- Pious Lion Pure Premium Potent White Maeng DA, Bright Uplift…
- Published
- June 20, 2018
- Distribution
- Product was distributed to NC & TN.
Pious Lion Recall: The firm was notified by the North Carolina Dept. of Agriculture that the product contains Salmonella.
United States
OngoingClass I
- Company
- Pious Lion
- Product
- Pious Lion Pure Premium Potent Limited Release Pink Bali, 1…
- Recall date
- May 18, 2018
- Source
- FDA
Reason for recall
The firm was notified by the North Carolina Dept. of Agriculture that the product contains Salmonella.
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Pious Lion Pure Premium Potent Limited Release Pink Bali, 1 oz plastic bag. 833-AVL-KRTM www.piouslion.com | Not published in this source record | 40/1oz plastic bags | There are no codes on the product. |
Distribution
- Product was distributed to NC & TN.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1546-2018
- Event ID
- 80151
- Status
- Ongoing
- Classification
- Class I
- Company
- Pious Lion
- Product description
- Pious Lion Pure Premium Potent Limited Release Pink Bali, 1 oz plastic bag. 833-AVL-KRTM www.piouslion.com
- Quantity
- 40/1oz plastic bags
- Reason
- The firm was notified by the North Carolina Dept. of Agriculture that the product contains Salmonella.
- Recall initiation date
- May 18, 2018
- Report date
- June 20, 2018
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Product was distributed to NC & TN.
- UPC, lot, and code information
- There are no codes on the product.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 80151 with 1 other product entry in Public Health Trace.
Responsible company: Pious Lion
Other recalls from Pious Lion
FDA Recall United States Ongoing Historical recordClass I
Pious Lion
- Product
- Pious Lion Pure Premium Potent White Maeng DA, Bright Uplift…
- Published
- June 20, 2018
- Distribution
- Product was distributed to NC & TN.
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.
| State | Distributed |
|---|---|
| North Carolina | 1 |
| Tennessee | 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.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
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?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Ongoing." 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 instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
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