Latitude 36 Foods Recall: Product contains undeclared Soy and Sesame
United States
TerminatedClass I
- Company
- Latitude 36 Foods
- Product
- Honey Balsamic dressing, 3.4 ounce plastic pouch, Best by d…
- Recall date
- August 21, 2025
- Terminated
- November 25, 2025
- Source
- FDA
Reason for recall
Product contains undeclared Soy and Sesame
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Honey Balsamic dressing, 3.4 ounce plastic pouch, Best by date and Lot number appear directly on pouch. | Not published in this source record | 46,800 units master packs across both lots | Lot: 131105-3335 & 131105-3335A |
Distribution
- Product was distributed to one customer in California.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0605-2025
- Event ID
- 97484
- Status
- Terminated
- Classification
- Class I
- Company
- Latitude 36 Foods
- Product description
- Honey Balsamic dressing, 3.4 ounce plastic pouch, Best by date and Lot number appear directly on pouch.
- Quantity
- 46,800 units master packs across both lots
- Reason
- Product contains undeclared Soy and Sesame
- Recall initiation date
- August 21, 2025
- Report date
- September 24, 2025
- Classification date
- Not published in this source record
- Termination date
- November 25, 2025
- Distribution pattern
- Product was distributed to one customer in California.
- UPC, lot, and code information
- Lot: 131105-3335 & 131105-3335A
- 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: Latitude 36 Foods
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 I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
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.
