FDA Recall United States Terminated Historical recordClass I
Fresh Express Incorpated
- Product
- Fresh Express Gourmet Cafe Chicken Caesar 5.75oz, Labeled Sa…
- Published
- December 11, 2024
- Distribution
- U.S. distribution within states in retai…
Fresh Express Incorpated Recall: Potential Listeria Monocytogenes Contamination. The pre-packaged condiment trays contains chicken linked to the Bruce Pac recall.
United States
TerminatedClass I
- Company
- Fresh Express Incorpated
- Product
- Fresh Express Gourmet Cafe Santa Fe Greek 5.2 oz, Labeled Sa…
- Recall date
- October 18, 2024
- Terminated
- December 31, 2024
- Source
- FDA
Reason for recall
Potential Listeria Monocytogenes Contamination. The pre-packaged condiment trays contains chicken linked to the Bruce Pac recall.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Fresh Express Gourmet Cafe Santa Fe Greek 5.2 oz, Labeled Salad Bowls, Refrigerate, UPC Code: 71279 40713 5 and Case Code :71279-56704 | Not published in this source record | 210 Cases | Lot Code: Z257, Z262, Z267, Z271 Expiration Date: 09/30/2024, 10/05/2024, 10/10/2024, 10/14/2024 |
Distribution
- U.S. distribution within states in retail locations in LA
- MO
- IL
- KY
- OH
- MN
- IN
- CA
- UT
- VT
- TX
- WI. No Foreign distribution.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0257-2025
- Event ID
- 95629
- Status
- Terminated
- Classification
- Class I
- Company
- Fresh Express Incorpated
- Product description
- Fresh Express Gourmet Cafe Santa Fe Greek 5.2 oz, Labeled Salad Bowls, Refrigerate, UPC Code: 71279 40713 5 and Case Code :71279-56704
- Quantity
- 210 Cases
- Reason
- Potential Listeria Monocytogenes Contamination. The pre-packaged condiment trays contains chicken linked to the Bruce Pac recall.
- Recall initiation date
- October 18, 2024
- Report date
- December 11, 2024
- Classification date
- Not published in this source record
- Termination date
- December 31, 2024
- Distribution pattern
- U.S. distribution within states in retail locations in LA, MO, IL, KY, OH, MN, IN, CA, UT, VT, TX, WI. No Foreign distribution.
- UPC, lot, and code information
- Lot Code: Z257, Z262, Z267, Z271 Expiration Date: 09/30/2024, 10/05/2024, 10/10/2024, 10/14/2024
- 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
Other products recalled under this same event
This recall shares FDA event ID 95629 with 1 other product entry in Public Health Trace.
Responsible company: Fresh Express Incorpated
Other recalls from Fresh Express Incorpated
FDA Recall United States Terminated Historical recordClass I
Fresh Express Incorpated
- Product
- Fresh Express Gourmet Cafe Chicken Caesar 5.75oz, Labeled Sa…
- Published
- December 11, 2024
- Distribution
- U.S. distribution within states in retai…
FDA Recall United States Terminated Historical recordClass I
Fresh Express Incorpated
- Product
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- Published
- February 21, 2024
- Distribution
- AL, FL, GA, CA, UT, WA; Canada
FDA Recall United States Terminated Historical recordClass I
Fresh Express Incorpated
- Product
- Chopped Salad Kit Southwest with condiments(toppings that in…
- Published
- February 21, 2024
- Distribution
- AL, FL, GA, CA, UT, WA; Canada
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 |
|---|---|
| Louisiana | 1 |
| Missouri | 1 |
| Illinois | 1 |
| Kentucky | 1 |
| Ohio | 1 |
| Minnesota | 1 |
| Indiana | 1 |
| California | 1 |
| Utah | 1 |
| Vermont | 1 |
| Texas | 1 |
| Wisconsin | 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 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.
