Quaker Manufacturing, LLC Recall: Product tested positive for Salmonella.
United States
TerminatedClass I
- Company
- Quaker Manufacturing, LLC
- Product
- Cap'n Crunch's Peanut Butter Crunch Cereal packaged in 17.1…
- Recall date
- November 13, 2018
- Terminated
- March 11, 2019
- Source
- FDA
Reason for recall
Product tested positive for Salmonella.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Cap'n Crunch's Peanut Butter Crunch Cereal packaged in 17.1 ounce and 16.5 ounce cardboard boxes. Distributed by The Quaker Oats Company, Chicago IL | Not published in this source record | 108 cases | Lots 110218L and 110318L |
Distribution
- Distributed to distribution centers in AR
- IA
- IL
- KS
- MO
- NE
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0718-2019
- Event ID
- 81571
- Status
- Terminated
- Classification
- Class I
- Company
- Quaker Manufacturing, LLC
- Product description
- Cap'n Crunch's Peanut Butter Crunch Cereal packaged in 17.1 ounce and 16.5 ounce cardboard boxes. Distributed by The Quaker Oats Company, Chicago IL
- Quantity
- 108 cases
- Reason
- Product tested positive for Salmonella.
- Recall initiation date
- November 13, 2018
- Report date
- December 19, 2018
- Classification date
- Not published in this source record
- Termination date
- March 11, 2019
- Distribution pattern
- Distributed to distribution centers in AR, IA, IL, KS, MO, NE
- UPC, lot, and code information
- Lots 110218L and 110318L
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Quaker Manufacturing, LLC
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 |
| Iowa | 1 |
| Illinois | 1 |
| Kansas | 1 |
| Missouri | 1 |
| Nebraska | 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.
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.
