FDA Recall United States Terminated Historical recordClass III
Elwood International, Inc.
- Product
- Calais Brand Grape jelly; 128 FL. OZ. (1 GAL.) 3.785 L; INGR…
- Published
- July 16, 2025
- Distribution
- NY and NJ
Elwood International, Inc. Recall: The firm does not have a scheduled process on file for this product.
United States
TerminatedClass II
- Company
- Elwood International, Inc.
- Product
- ELWOOD FAT-FREE LOW SODIUM RANCH DRESSING ARTIFICIAL FLAVOR.…
- Recall date
- January 26, 2018
- Terminated
- August 1, 2018
- Source
- FDA
Reason for recall
The firm does not have a scheduled process on file for this product.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| ELWOOD FAT-FREE LOW SODIUM RANCH DRESSING ARTIFICIAL FLAVOR. Single serve. | Not published in this source record | 106 cases | All lots within expiry. |
Distribution
- Montana
- Illinois
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0791-2018
- Event ID
- 79034
- Status
- Terminated
- Classification
- Class II
- Company
- Elwood International, Inc.
- Product description
- ELWOOD FAT-FREE LOW SODIUM RANCH DRESSING ARTIFICIAL FLAVOR. Single serve.
- Quantity
- 106 cases
- Reason
- The firm does not have a scheduled process on file for this product.
- Recall initiation date
- January 26, 2018
- Report date
- February 14, 2018
- Classification date
- Not published in this source record
- Termination date
- August 1, 2018
- Distribution pattern
- Montana, Illinois
- UPC, lot, and code information
- All lots within expiry.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Elwood International, Inc.
Other recalls from Elwood International, 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 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.
