MAGNOLIA VEGETABLE PROCESSORS Recall: Wrong Label applied to Product.
United States
TerminatedClass III
- Company
- MAGNOLIA VEGETABLE PROCESSORS
- Product
- Wickles Relish 16oz glass jars - 6 jars per case
- Recall date
- July 20, 2021
- Terminated
- August 18, 2021
- Source
- FDA
Reason for recall
Wrong Label applied to Product.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Wickles Relish 16oz glass jars - 6 jars per case | Not published in this source record | 2904 cases | Lot No. 2001210406 Product No. 2001 Best By 04/06/24 |
Distribution
- Distributed to the following states: IL
- KY
- LA
- ME
- MD
- NC
- PA
- VA
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0859-2021
- Event ID
- 88316
- Status
- Terminated
- Classification
- Class III
- Company
- MAGNOLIA VEGETABLE PROCESSORS
- Product description
- Wickles Relish 16oz glass jars - 6 jars per case
- Quantity
- 2904 cases
- Reason
- Wrong Label applied to Product.
- Recall initiation date
- July 20, 2021
- Report date
- August 18, 2021
- Classification date
- Not published in this source record
- Termination date
- August 18, 2021
- Distribution pattern
- Distributed to the following states: IL, KY, LA, ME, MD, NC, PA, VA
- UPC, lot, and code information
- Lot No. 2001210406 Product No. 2001 Best By 04/06/24
- 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: MAGNOLIA VEGETABLE PROCESSORS
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 |
|---|---|
| Illinois | 1 |
| Kentucky | 1 |
| Louisiana | 1 |
| Maine | 1 |
| Maryland | 1 |
| North Carolina | 1 |
| Pennsylvania | 1 |
| Virginia | 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.
