Prairie City Bakery Recall: Salmonella. Product contains recalled Jif peanut butter as ingredient.
United States
TerminatedClass I
- Company
- Prairie City Bakery
- Product
- Prairie City Bakery Peanut Butter Chocolate Chip Ooey Gooey…
- Recall date
- June 3, 2022
- Terminated
- November 9, 2023
- Source
- FDA
Reason for recall
Salmonella. Product contains recalled Jif peanut butter as ingredient.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Prairie City Bakery Peanut Butter Chocolate Chip Ooey Gooey Butter Cake 2oz. individual UPC: 7-9788436718-2; 10 individual units per display unit; 6 display units per wholesale case. | 7-9788436718-2 | 626 cases | 1357-1: Best by 6/23/2023 and 2085-1: Best by: 9/25/2023 |
Distribution
- sold at gas stations and convenience stores nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1402-2022
- Event ID
- 90416
- Status
- Terminated
- Classification
- Class I
- Company
- Prairie City Bakery
- Product description
- Prairie City Bakery Peanut Butter Chocolate Chip Ooey Gooey Butter Cake 2oz. individual UPC: 7-9788436718-2; 10 individual units per display unit; 6 display units per wholesale case.
- Quantity
- 626 cases
- Reason
- Salmonella. Product contains recalled Jif peanut butter as ingredient.
- Recall initiation date
- June 3, 2022
- Report date
- July 13, 2022
- Classification date
- Not published in this source record
- Termination date
- November 9, 2023
- Distribution pattern
- sold at gas stations and convenience stores nationwide
- UPC, lot, and code information
- UPC 7-9788436718-2; 1357-1: Best by 6/23/2023 and 2085-1: Best by: 9/25/2023
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Prairie City Bakery
Where this information comes from
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.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
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.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
