Recalls / Class I
Class IF-0268-2025
Product
Whole and Cut Cucumbers packaged in the following sizes: 1. Select 40-45 lb. boxes Item 05000. 2. Bix 1/5 lb. Item 05023. 3. Bix Cucumber Dice 1/34" Skin-On 1/5 lb. Item 11861. 4. Bix Cucumber Dice 1/4" Seedless Skin-On. Item 11870. 5. Bix Cucumber Dice 1/2" Seedless Skin-On 1/5 lb. Item 11874. 6. Bix Cucumber Dice 3/8" Skin-On 1/5lb. Item 11890. 7. Bix Cucumber Dice 1/2" Skin-On 1/5 lb. Item 11895. 8. Bix Cucumber 1/2 Moon 1/2 Seedless Skin-On 1/5 lb. Item 11898. 9. Bix Cucumber 1/2" Dice Skin-Off Seedless 1/5 lb. Item11899. 10. Bix Cucumber 1/2 Moon1/4" Skin-On 1/5 lb. Item 11918. 11. Bix Cucumber Slice KK 3/16" Skin-On 1/5 lb. Item 11920. 12. Bix Cucumber Slice 1/4" Skin-On 1/5 lb. Item 11930. 13. Bix Cucumber Slice 1/4" Skin-On 4/5 lb. Item 11931. 14. Bix Cucumber Slice KK 3/16" Skin-On 1/15 lb. Item 11955. 15. Cucumber Fresh Select Keep Refrigerated. Item 47004.
- Type
- Food
- Affected lot / code info
- 1. Delivery Date 11/11/2024 2. Delivery date 11/11/2024 through11/13/2024 3. Julian Dates 24312 and24315 4. Julian Date 24315 5. Julian Dates 24314 and24315 6. Julian Dates 24314 and24315 7. Julian Dates 24313 and24315 8. Julian Dates 24309 and24315 9. Julian Date 24315 10. Julian Date 24315 11. Julian Dates 24312 and24316 12. Julian Dates 24313,24314, 24316, and24317 13. Julian Dates 24311,24314, 24315, 24316,and 24319 14. Julian Date 24314 15. Delivery Date11/12/2024
- Quantity
- 1065 cases
Why it was recalled
Cucumbers have the potential to be contaminated with Salmonella.
Recalling firm
- Firm
- Sysco Corporation
- Notification channel
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Type
- Voluntary: Firm initiated
- Address
- 1390 Enclave Pkwy, Houston, Texas 77077-2025
Distribution
- Distribution pattern
- IA, MN, SD, ND, WI. Outside the US to Canada
Timeline
- Recall initiated
- 2024-11-30
- FDA classified
- 2024-12-11
- Posted by FDA
- 2024-12-18
- Terminated
- 2025-02-07
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-0268-2025. The FDA issues recall classifications as health-hazard assessments, not legal findings.