Spice House Recall: Undeclared sesame
United States
TerminatedClass II
- Company
- Spice House
- Product
- The Spice House Sichuan Chile BBQ Rub 2.7oz glass jar UPC 81…
- Recall date
- November 18, 2021
- Terminated
- February 15, 2022
- Source
- FDA
Reason for recall
Undeclared sesame
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| The Spice House Sichuan Chile BBQ Rub 2.7oz glass jar UPC 816328028240 | 816328028240 | 737 units | No lot codes on product |
Distribution
- The product was only available for purchase from November 12 through November 18
- 2021. The product is distributed nationally through online sales via www.thespicehouse.com and also is sold at the four The Spice House retail locations in Illinois and Wisconsin.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0281-2022
- Event ID
- 89091
- Status
- Terminated
- Classification
- Class II
- Company
- Spice House
- Product description
- The Spice House Sichuan Chile BBQ Rub 2.7oz glass jar UPC 816328028240
- Quantity
- 737 units
- Reason
- Undeclared sesame
- Recall initiation date
- November 18, 2021
- Report date
- December 15, 2021
- Classification date
- Not published in this source record
- Termination date
- February 15, 2022
- Distribution pattern
- The product was only available for purchase from November 12 through November 18, 2021. The product is distributed nationally through online sales via www.thespicehouse.com and also is sold at the four The Spice House retail locations in Illinois and Wisconsin.
- UPC, lot, and code information
- UPC 816328028240; No lot codes on product
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Spice House
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.
