Choice Products LLC. Recall: Peanut Butter Cookie Dough may contain undeclared milk.
United States
TerminatedClass I
- Company
- Choice Products LLC.
- Product
- Premiere Choice 3lb. Peanut Butter Cookie Dough, item 412, N…
- Recall date
- February 26, 2020
- Terminated
- September 28, 2020
- Source
- FDA
Reason for recall
Peanut Butter Cookie Dough may contain undeclared milk.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Premiere Choice 3lb. Peanut Butter Cookie Dough, item 412, Net Wt. 48 oz (1360g) UPC 6 98240 00412 6. Made by: Club's Choice Fundraising, Eau Claire, WI 54703 | Not published in this source record | 275 - 3lb. tubs | date code 19330 |
Distribution
- Nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0796-2020
- Event ID
- 85088
- Status
- Terminated
- Classification
- Class I
- Company
- Choice Products LLC.
- Product description
- Premiere Choice 3lb. Peanut Butter Cookie Dough, item 412, Net Wt. 48 oz (1360g) UPC 6 98240 00412 6. Made by: Club's Choice Fundraising, Eau Claire, WI 54703
- Quantity
- 275 - 3lb. tubs
- Reason
- Peanut Butter Cookie Dough may contain undeclared milk.
- Recall initiation date
- February 26, 2020
- Report date
- March 11, 2020
- Classification date
- Not published in this source record
- Termination date
- September 28, 2020
- Distribution pattern
- Nationwide
- UPC, lot, and code information
- date code 19330
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Choice Products LLC.
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.
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