FDA Recall United States Terminated Historical recordClass II
EL Chilar Huff
- Product
- El Chilar Whole Ginger, NET WT 1.25 Oz (35g)
- Published
- September 27, 2017
- Distribution
- U.S. Consignees only.
EL Chilar Huff Recall: Sample collected by NY Department of Agriculture tested positive for high levels of lead (2.39 ppm) in ground cinnamon.
United States
TerminatedClass II
- Company
- EL Chilar Huff
- Product
- Lisy Ground Cinnamon Canela Molida NET WT./CONT. NETO 13 OZ…
- Recall date
- June 26, 2019
- Terminated
- January 23, 2020
- Source
- FDA
Reason for recall
Sample collected by NY Department of Agriculture tested positive for high levels of lead (2.39 ppm) in ground cinnamon.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Lisy Ground Cinnamon Canela Molida NET WT./CONT. NETO 13 OZ (368g) and 2 OZ (57g) | Not published in this source record | 1266 jars of lot E352; 1680 jars of lot E360; 384 (2 oz) jars of E360 i | ITEM 1113; UPC 096786300137; LOTS E352 and E360; Exp 2021 ITEM 814; UPC 096786600534; LOT E360 |
Distribution
- Product sent to distributors in FL
- NC
- MD and NJ
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1947-2019
- Event ID
- 83238
- Status
- Terminated
- Classification
- Class II
- Company
- EL Chilar Huff
- Product description
- Lisy Ground Cinnamon Canela Molida NET WT./CONT. NETO 13 OZ (368g) and 2 OZ (57g)
- Quantity
- 1266 jars of lot E352; 1680 jars of lot E360; 384 (2 oz) jars of E360 i
- Reason
- Sample collected by NY Department of Agriculture tested positive for high levels of lead (2.39 ppm) in ground cinnamon.
- Recall initiation date
- June 26, 2019
- Report date
- July 31, 2019
- Classification date
- Not published in this source record
- Termination date
- January 23, 2020
- Distribution pattern
- Product sent to distributors in FL, NC, MD and NJ
- UPC, lot, and code information
- ITEM 1113; UPC 096786300137; LOTS E352 and E360; Exp 2021 ITEM 814; UPC 096786600534; LOT E360
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: EL Chilar Huff
Other recalls from EL Chilar Huff
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 |
|---|---|
| Florida | 1 |
| North Carolina | 1 |
| Maryland | 1 |
| New Jersey | 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 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.
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