Garden Vegetable Cream Cheese Spread. Net Wt 8 oz. (226g). Keep Refrigerated, packaged under…
Recalling firm: Schreiber Foods Inc
Potential Salmonella contamination.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Aug 8, 2024.
Check your package
Compare the exact product and package details with the label you have.
021333830539, 041303006252, 041318580051, 070253501005, 075450096064FDA code information
1. USE BY SEP 13 24, USE BY SEP 22 24, USE BY SEP 01 24 2. BEST BY 09/01/24 3. BEST BY 08/08/24 4. BEST BY 09/13/24, BEST BY 09/22/24 5. BEST BY 09/01/24
Match the product, package size, and code together. A missing match does not guarantee safety.
Full FDA record and distribution details
Original product description
Garden Vegetable Cream Cheese Spread. Net Wt 8 oz. (226g). Keep Refrigerated, packaged under the following brands: 1. Fareway, UPC 0 21333-83053 9. Packed for Fareway Store, Inc. Boone, Iowa 50036. 2. Essential Everyday, UPC 0 41303-00625 2. Distributed By Supervalu Inc., Eden Prairie, MN 55344. 3. Schnuck, UPC 0 41318-58005 1. Distributed By Schnuck Markets, Inc., St. Louis, MO 63146-6928. 4. Hy Vee, UPC 0 75450-09606 4. Distributed By Hy-Vee Inc. West Des Moines, IA 50266. 5. Our Family, UPC 0 70253-50100 5. Distributed By Pique Brands, Inc. Grand Rapids, MI 49518.
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 021333830539 | (226g). Keep Refrigerated, packaged under the following brands: 1. Fareway, UPC 0 21333-83053 9. Packed for Fareway Store, Inc. Boone, Iowa 50036. 2. Essential Everyday, UPC 0 41303-00625 2. Distributed By Superva |
| UPC | 041303006252 | Packed for Fareway Store, Inc. Boone, Iowa 50036. 2. Essential Everyday, UPC 0 41303-00625 2. Distributed By Supervalu Inc., Eden Prairie, MN 55344. 3. Schnuck, UPC 0 41318-58005 1. Distributed By Schnuck Markets |
| UPC | 041318580051 | 00625 2. Distributed By Supervalu Inc., Eden Prairie, MN 55344. 3. Schnuck, UPC 0 41318-58005 1. Distributed By Schnuck Markets, Inc., St. Louis, MO 63146-6928. 4. Hy Vee, UPC 0 75450-09606 4. Distributed By Hy-V |
| UPC | 070253501005 | 606 4. Distributed By Hy-Vee Inc. West Des Moines, IA 50266. 5. Our Family, UPC 0 70253-50100 5. Distributed By Pique Brands, Inc. Grand Rapids, MI 49518. |
| UPC | 075450096064 | stributed By Schnuck Markets, Inc., St. Louis, MO 63146-6928. 4. Hy Vee, UPC 0 75450-09606 4. Distributed By Hy-Vee Inc. West Des Moines, IA 50266. 5. Our Family, UPC 0 70253-50100 5. Distributed By Pique Brands, |
| best by | 08/08/24 | BY SEP 13 24, USE BY SEP 22 24, USE BY SEP 01 24 2. BEST BY 09/01/24 3. BEST BY 08/08/24 4. BEST BY 09/13/24, BEST BY 09/22/24 5. BEST BY 09/01/24 |
| best by | 09/01/24 | 1. USE BY SEP 13 24, USE BY SEP 22 24, USE BY SEP 01 24 2. BEST BY 09/01/24 3. BEST BY 08/08/24 4. BEST BY 09/13/24, BEST BY 09/22/24 5. BEST BY 09/01/24 |
| best by | 09/01/24 | Y 09/01/24 3. BEST BY 08/08/24 4. BEST BY 09/13/24, BEST BY 09/22/24 5. BEST BY 09/01/24 |
| best by | 09/13/24 | SEP 22 24, USE BY SEP 01 24 2. BEST BY 09/01/24 3. BEST BY 08/08/24 4. BEST BY 09/13/24, BEST BY 09/22/24 5. BEST BY 09/01/24 |
| best by | 09/22/24 | SEP 01 24 2. BEST BY 09/01/24 3. BEST BY 08/08/24 4. BEST BY 09/13/24, BEST BY 09/22/24 5. BEST BY 09/01/24 |
Original FDA recall reason
Potential Salmonella contamination.
Recall details
- Recall number
- F-1291-2024
- Event ID
- 94578
- FDA status
- Terminated
- Initiated
- May 3, 2024
- Reported
- Jun 12, 2024
- Classified
- Jun 4, 2024
- Terminated
- Aug 8, 2024
- Quantity
- 835,721 units total (all products)
- Location
- Green Bay, WI, 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
CA, FL, IA, IL, IN, MA, MD, MI, MN, MO, NC, NJ, NY, OH, PA, TX, VA, WA, WI. Product was also shipped to Puerto Rico.
Data updated September 16, 2026. View official FDA data ↗
Follow official FDA and manufacturer guidance.