FDA Recall United States Terminated Historical recordClass II
Rich Products Corp
- Product
- ARTISAN CRUST PIZZA DOUGH 24/18, PRODUCT CODE 11413, UPC 1 0…
- Published
- May 31, 2017
- Distribution
- Multiple states
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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass II
The product was made with flour supplied by Ardent Mills who issued a recall on flour products due to possible E. coli 0121 contamination.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 7 OZ PIZZA DOUGH BALL, PRODUCT CODE 11267, UPC 0 00 49800 1267 4, NET CASE WT 12.9 KG (28 LB 7 OZ), UNIT NET WT: 198 G (7 OZ), COUNT: 65 --- PROCESSED IN CANADA, DIST. BY RICH PRODUCTS CORPORATION, BUFFALO, N.Y. 14213 U.S.A. | Not published in this source record | 13,043 cases US (total for all products) | Lot 77006354, Use By 18/Apr/17; Lot 77006355, Use By 19/Apr/17; Lot 77007009, Use By 9/May/17; Lot 77007010, Use By 10/May/17; Lot 77007016, Use by 16/May/17; Lot 77007023, Use by 23/May/17; Lot 77007024, Use by 24/May/17; Lot 77007031, Use by 31/May/17; Lot 77007045, Use by 14/Jun/17; 77007058, Use by 27/Jun/17; Lot 77007059, Use by 28/Jun/17; Lot 77007072, Use by 11/Jun/17; Lot 77007073, Use by 12/Jun/17. |
This recall shares FDA event ID 77153 with 2 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
Responsible company: Rich Products Corp
FDA Recall United States Ongoing 2026 recordClass II
FDA Recall United States Terminated 2026 recordClass II
FDA Recall United States Terminated Historical recordClass I
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 |
|---|---|
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Kentucky | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Maine | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| North Carolina | 1 |
| Nebraska | 1 |
| New Jersey | 1 |
| New Mexico | 1 |
| New York | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Washington | 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.
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.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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.
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