Able Sales Company, Inc. Recall: Traces of 2-chloro-ethanol (2-CE) in wheat gluten.
United States
TerminatedClass III
- Company
- Able Sales Company, Inc.
- Product
- Tereos Wheat Gluten, Net Weight 50 lbs, Distributed by Meelu…
- Recall date
- April 5, 2022
- Terminated
- June 9, 2022
- Source
- FDA
Reason for recall
Traces of 2-chloro-ethanol (2-CE) in wheat gluten.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Tereos Wheat Gluten, Net Weight 50 lbs, Distributed by Meelunie, Produced in France | Not published in this source record | 8,000 bags/50 lb each | Batch Numbers: F2I252411 F2I252431 F2I252441 F2I252451 F2J112411 F2J183404 F2J193401 F2J197404 F2J249413 F2J256401 |
Distribution
- Domestic distribution only - PR
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1082-2022
- Event ID
- 89980
- Status
- Terminated
- Classification
- Class III
- Company
- Able Sales Company, Inc.
- Product description
- Tereos Wheat Gluten, Net Weight 50 lbs, Distributed by Meelunie, Produced in France
- Quantity
- 8,000 bags/50 lb each
- Reason
- Traces of 2-chloro-ethanol (2-CE) in wheat gluten.
- Recall initiation date
- April 5, 2022
- Report date
- June 1, 2022
- Classification date
- Not published in this source record
- Termination date
- June 9, 2022
- Distribution pattern
- Domestic distribution only - PR
- UPC, lot, and code information
- Batch Numbers: F2I252411 F2I252431 F2I252441 F2I252451 F2J112411 F2J183404 F2J193401 F2J197404 F2J249413 F2J256401
- 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: Able Sales Company, Inc.
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 |
|---|---|
| Puerto Rico | 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 III mean?
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
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.
