Fresh Express Gourmet Cafe Santa Fe Greek 5.2 oz, Labeled Salad Bowls, Refrigerate
Recalling firm: Fresh Express Incorpated
Why it was recalled
Potential Listeria Monocytogenes Contamination. The pre-packaged condiment trays contains chicken linked to the Bruce Pac recall.
The exact product
Fresh Express Gourmet Cafe Santa Fe Greek 5.2 oz, Labeled Salad Bowls, Refrigerate, UPC Code: 71279 40713 5 and Case Code :71279-56704
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
Lot Code: Z257, Z262, Z267, Z271 Expiration Date: 09/30/2024, 10/05/2024, 10/10/2024, 10/14/2024
| Type | Code / value | Context |
|---|---|---|
| expiration | 09/30/2024 | Lot Code: Z257, Z262, Z267, Z271 Expiration Date: 09/30/2024, 10/05/2024, 10/10/2024, 10/14/2024 |
| lot | Z257 | Lot Code: Z257, Z262, Z267, Z271 Expiration Date: 09/30/2024, 10/05/2024, 10/10/2024, 10/14/2024 |
| lot | Z262 | Lot Code: Z257, Z262, Z267, Z271 Expiration Date: 09/30/2024, 10/05/2024, 10/10/2024, 10/14/2024 |
| lot | Z267 | Lot Code: Z257, Z262, Z267, Z271 Expiration Date: 09/30/2024, 10/05/2024, 10/10/2024, 10/14/2024 |
| lot | Z271 | Lot Code: Z257, Z262, Z267, Z271 Expiration Date: 09/30/2024, 10/05/2024, 10/10/2024, 10/14/2024 |
Recall details
- Recall number
- F-0257-2025
- Event ID
- 95629
- FDA status
- Terminated
- Initiated
- Oct 18, 2024
- Reported
- Dec 11, 2024
- Classified
- Dec 5, 2024
- Terminated
- Dec 31, 2024
- Quantity
- 210 Cases
- Location
- Windermere, FL, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
U.S. distribution within states in retail locations in LA, MO, IL, KY, OH, MN, IN, CA, UT, VT, TX, WI. No Foreign distribution.
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.