Aroma Imports Inc Recall: Elevated lead levels in product
United States
TerminatedClass I
- Company
- Aroma Imports Inc
- Product
- Nabelsi Thyme (also known on invoices as Zatar) 450g retail…
- Recall date
- March 17, 2017
- Terminated
- December 5, 2017
- Source
- FDA
Reason for recall
Elevated lead levels in product
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Nabelsi Thyme (also known on invoices as Zatar) 450g retail (24 packages per wholesale case) 4.5kg retail (2 bags per wholesale case) Cardboard box wholesale case, retail packages flexible plastic | Not published in this source record | 95 cases of 24(450g), 10 cases of 2 bags(4.5kg) | Pro. Date: 8/20/2016 Exp. Date: 8/20/2018 |
Distribution
- Illinois
- Michigan
- Ohio
- Virginia
- and New Jersey
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-2180-2017
- Event ID
- 76993
- Status
- Terminated
- Classification
- Class I
- Company
- Aroma Imports Inc
- Product description
- Nabelsi Thyme (also known on invoices as Zatar) 450g retail (24 packages per wholesale case) 4.5kg retail (2 bags per wholesale case) Cardboard box wholesale case, retail packages flexible plastic
- Quantity
- 95 cases of 24(450g), 10 cases of 2 bags(4.5kg)
- Reason
- Elevated lead levels in product
- Recall initiation date
- March 17, 2017
- Report date
- May 10, 2017
- Classification date
- Not published in this source record
- Termination date
- December 5, 2017
- Distribution pattern
- Illinois, Michigan, Ohio, Virginia, and New Jersey
- UPC, lot, and code information
- Pro. Date: 8/20/2016 Exp. Date: 8/20/2018
- 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
Responsible company: Aroma Imports Inc
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 "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.
