FDA Recall United States Terminated Historical recordClass II
UNFI General Corporate
- Product
- 1. S.AMERICA OG1 ANJOU PEAR LG
- Published
- July 16, 2025
- Distribution
- Multiple states
UNFI General Corporate Recall: Product was found positive for Salmonella
United States
TerminatedClass II
- Company
- UNFI General Corporate
- Product
- Essential Everyday, Unbleached Flour, Enriched All-Purpose P…
- Recall date
- December 13, 2019
- Terminated
- March 17, 2020
- Source
- FDA
Reason for recall
Product was found positive for Salmonella
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Essential Everyday, Unbleached Flour, Enriched All-Purpose Pre-Sifted, packaged in a 5lb paper bag | Not published in this source record | 1440 bags | Lot code 481123- Best by date 12/07/2020 |
Distribution
- The firm distributed this product to one consignee
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0561-2020
- Event ID
- 84552
- Status
- Terminated
- Classification
- Class II
- Company
- UNFI General Corporate
- Product description
- Essential Everyday, Unbleached Flour, Enriched All-Purpose Pre-Sifted, packaged in a 5lb paper bag
- Quantity
- 1440 bags
- Reason
- Product was found positive for Salmonella
- Recall initiation date
- December 13, 2019
- Report date
- February 5, 2020
- Classification date
- Not published in this source record
- Termination date
- March 17, 2020
- Distribution pattern
- The firm distributed this product to one consignee
- UPC, lot, and code information
- Lot code 481123- Best by date 12/07/2020
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: UNFI General Corporate
Other recalls from UNFI General Corporate
FDA Recall United States Terminated Historical recordClass II
UNFI General Corporate
- Product
- 1. USA OG2 SDLS MINI WTRM
- Published
- July 16, 2025
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass II
UNFI General Corporate
- Product
- 1.MIGHTIES OG2 KIWI
- Published
- July 16, 2025
- Distribution
- Multiple states
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.
