FDA Recall United States Terminated Historical recordClass I
Vanlaw Food Products, Inc
- Product
- WFM 365 Organic Creamy Caesar, 12oz, UPC#99482490290, Keep R…
- Published
- April 27, 2022
- Distribution
- Multiple states
Vanlaw Food Products, Inc Recall: Product does not declare the allergens of wheat and soy on label.
United States
TerminatedClass II
- Company
- Vanlaw Food Products, Inc
- Product
- WFM 365 Organic Creamy Caesar, 12oz, UPC#: 99482490029, Keep…
- Recall date
- August 25, 2022
- Terminated
- April 28, 2023
- Source
- FDA
Reason for recall
Product does not declare the allergens of wheat and soy on label.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| WFM 365 Organic Creamy Caesar, 12oz, UPC#: 99482490029, Keep Refrigerated. Bottled in USA. Distributed by: Whole Foods Market: Austin, TX Expanded recall to include the best if used by date of SEP 21 22 through JUN 06 23 and UPC Code 99482-49027 | Not published in this source record | 31,858 units | Lot Code: Top Line Code: 04 06 23, which indicates that the product is best if used by date of SEP 21 22 through JUN 06 23 and UPC Code 99482-49027. Bottom Line Code: A535-1, which is the identification code of the product |
Distribution
- Product was distributed to 4 distribution centers located in FL
- WI
- CO
- and NY. Product was further distributed to Alabama
- Connecticut
- Georgia
- Illinois
- Indiana
- Iowa
- Kansas
- Kentucky
- Michigan
- Minnesota
- Mississippi
- Missouri
- Nebraska
- New Jersey
- New Mexico
- North Carolina
- Ohio
- South Carolina
- Tennessee
- Texas
- Utah
- and Wyoming.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0002-2023
- Event ID
- 90806
- Status
- Terminated
- Classification
- Class II
- Company
- Vanlaw Food Products, Inc
- Product description
- WFM 365 Organic Creamy Caesar, 12oz, UPC#: 99482490029, Keep Refrigerated. Bottled in USA. Distributed by: Whole Foods Market: Austin, TX Expanded recall to include the best if used by date of SEP 21 22 through JUN 06 23 and UPC Code 99482-49027
- Quantity
- 31,858 units
- Reason
- Product does not declare the allergens of wheat and soy on label.
- Recall initiation date
- August 25, 2022
- Report date
- October 12, 2022
- Classification date
- Not published in this source record
- Termination date
- April 28, 2023
- Distribution pattern
- Product was distributed to 4 distribution centers located in FL, WI, CO, and NY. Product was further distributed to Alabama, Connecticut, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Michigan, Minnesota, Mississippi, Missouri, Nebraska, New Jersey, New Mexico, North Carolina, Ohio, South Carolina, Tennessee, Texas, Utah, and Wyoming.
- UPC, lot, and code information
- Lot Code: Top Line Code: 04 06 23, which indicates that the product is best if used by date of SEP 21 22 through JUN 06 23 and UPC Code 99482-49027. Bottom Line Code: A535-1, which is the identification code of the product
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Vanlaw Food Products, Inc
Other recalls from Vanlaw Food Products, Inc
FDA Recall United States Terminated Historical recordClass I
Vanlaw Food Products, Inc
- Product
- Winco Foods Creamy Ranch Dressing 16 fl oz. UPC Code: 0 7…
- Published
- January 11, 2017
- Distribution
- U.S. distribution to the following; OR,…
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 |
| Wisconsin | 1 |
| Colorado | 1 |
| New York | 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.
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.
