Something South African LLC Recall: Due to presence of mold (Aspergillus brasiliensis) and Ochratoxin A.
United States
TerminatedClass II
- Company
- Something South African LLC
- Product
- Pepper Collection 8 Tube Gift Set - a colorful assortment of…
- Recall date
- December 12, 2022
- Terminated
- April 24, 2023
- Source
- FDA
Reason for recall
Due to presence of mold (Aspergillus brasiliensis) and Ochratoxin A.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Pepper Collection 8 Tube Gift Set - a colorful assortment of dried peppers. This product contains peppers in 8 different glass tube and packaged in a printed paperboard sleeve and are visible through a window in the sleeve. Net wt. is 4.87oz/138g. The UPC is 6 009686 793712. Packed in South Africa. US Importer: Something South African, LLC Seattle WA 98199, Email: info@somethingsouthafrican.net. | Not published in this source record | 4200 units | BBE: JUN/2024. Batch: 494951 -T |
Distribution
- nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0263-2023
- Event ID
- 91329
- Status
- Terminated
- Classification
- Class II
- Company
- Something South African LLC
- Product description
- Pepper Collection 8 Tube Gift Set - a colorful assortment of dried peppers. This product contains peppers in 8 different glass tube and packaged in a printed paperboard sleeve and are visible through a window in the sleeve. Net wt. is 4.87oz/138g. The UPC is 6 009686 793712. Packed in South Africa. US Importer: Something South African, LLC Seattle WA 98199, Email: info@somethingsouthafrican.net.
- Quantity
- 4200 units
- Reason
- Due to presence of mold (Aspergillus brasiliensis) and Ochratoxin A.
- Recall initiation date
- December 12, 2022
- Report date
- January 25, 2023
- Classification date
- Not published in this source record
- Termination date
- April 24, 2023
- Distribution pattern
- nationwide
- UPC, lot, and code information
- BBE: JUN/2024. Batch: 494951 -T
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Something South African LLC
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 II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." 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?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
