Three Cheese Pasta Spinache Stonemill Kitchens, item # 71117.19500, 2/5 # packages.
Recalling firm: Reser's Fine Foods, Inc.
Three Cheese Pasta Spinache Stonemill Kitchens is recalled due to a potential contamination with Cyclospora. The pasta salad contains spinach that was recalled due to a potential…
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: Nov 5, 2018.
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071117195002FDA code information
Expiration date 9/11/2018, Lot # 180911010 Expiration date 9/15/2018, Lot # 180915010
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Full FDA record and distribution details
Original product description
Three Cheese Pasta Spinache Stonemill Kitchens, item # 71117.19500, 2/5 # packages. UPC 0 71117 19500 2. Product is pasta salads with vinaigrette dressings and vegetables including spinach. All products are in white plastic tubs with labeled lids packed 2/5 # to a corrugated case. Product is not labeled for retail sale. Refrigerated and ready to eat product.
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 071117195002 | se Pasta Spinache Stonemill Kitchens, item # 71117.19500, 2/5 # packages. UPC 0 71117 19500 2. Product is pasta salads with vinaigrette dressings and vegetables including spinach. All products are in white pla |
| expiration | 9/11/2018 | Expiration date 9/11/2018, Lot # 180911010 Expiration date 9/15/2018, Lot # 180915010 |
| expiration | 9/15/2018 | Expiration date 9/11/2018, Lot # 180911010 Expiration date 9/15/2018, Lot # 180915010 |
| lot | 180911010 | Expiration date 9/11/2018, Lot # 180911010 Expiration date 9/15/2018, Lot # 180915010 |
| lot | 180915010 | Expiration date 9/11/2018, Lot # 180911010 Expiration date 9/15/2018, Lot # 180915010 |
Original FDA recall reason
Three Cheese Pasta Spinache Stonemill Kitchens is recalled due to a potential contamination with Cyclospora. The pasta salad contains spinach that was recalled due to a potential contamination with Cyclospora.
Recall details
- Recall number
- F-1848-2018
- Event ID
- 80858
- FDA status
- Terminated
- Initiated
- Aug 17, 2018
- Reported
- Aug 29, 2018
- Classified
- Aug 23, 2018
- Terminated
- Nov 5, 2018
- Quantity
- 423 cases
- Location
- Beaverton, OR, 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
Distributed in AZ, CA, GA, ID, KS, MI, MT, NV, OK, OR, TX, UT, and WA. International country including CANADA
Data updated September 16, 2026. View official FDA data ↗
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