FRESHPOINT CENTRAL FLORIDA, INC. Recall: Mislabeled salads (undeclared peanut allergen). Incorrect ingredient applied (peanuts)
United States
TerminatedClass I
- Company
- FRESHPOINT CENTRAL FLORIDA, INC.
- Product
- Garden Salad 5 oz Lot # 6620223 Best By: 02.05, UPC 7663757…
- Recall date
- January 28, 2025
- Terminated
- July 1, 2026
- Source
- FDA
Reason for recall
Mislabeled salads (undeclared peanut allergen). Incorrect ingredient applied (peanuts)
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Garden Salad 5 oz Lot # 6620223 Best By: 02.05, UPC 766375733300 | 766375733300 | 18 units | Lot # 6620223 Best By: 02.05, UPC 766375733300 |
Distribution
- Florida and Georgia
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0577-2025
- Event ID
- 96211
- Status
- Terminated
- Classification
- Class I
- Company
- FRESHPOINT CENTRAL FLORIDA, INC.
- Product description
- Garden Salad 5 oz Lot # 6620223 Best By: 02.05, UPC 766375733300
- Quantity
- 18 units
- Reason
- Mislabeled salads (undeclared peanut allergen). Incorrect ingredient applied (peanuts)
- Recall initiation date
- January 28, 2025
- Report date
- March 5, 2025
- Classification date
- Not published in this source record
- Termination date
- July 1, 2026
- Distribution pattern
- Florida and Georgia
- UPC, lot, and code information
- UPC 766375733300; Lot # 6620223 Best By: 02.05, UPC 766375733300
- 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: FRESHPOINT CENTRAL FLORIDA, 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 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.
