Anderson's Frozen Custard Recall: The Pumpkin Ice Cream Pies may contain undeclared peanuts.
United States
TerminatedClass I
- Company
- Anderson's Frozen Custard
- Product
- Andersons Pumpkin Pie ice cream pie, 8 inch round ice cream…
- Recall date
- November 23, 2016
- Terminated
- January 12, 2017
- Source
- FDA
Reason for recall
The Pumpkin Ice Cream Pies may contain undeclared peanuts.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Andersons Pumpkin Pie ice cream pie, 8 inch round ice cream pie with whipped frosting --- The pie is packaged in a 9 inch round clear plastic dome container | Not published in this source record | 102 pies | All lots (product is seasonal: September-November) |
Distribution
- New York
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1229-2017
- Event ID
- 75804
- Status
- Terminated
- Classification
- Class I
- Company
- Anderson's Frozen Custard
- Product description
- Andersons Pumpkin Pie ice cream pie, 8 inch round ice cream pie with whipped frosting --- The pie is packaged in a 9 inch round clear plastic dome container
- Quantity
- 102 pies
- Reason
- The Pumpkin Ice Cream Pies may contain undeclared peanuts.
- Recall initiation date
- November 23, 2016
- Report date
- January 18, 2017
- Classification date
- Not published in this source record
- Termination date
- January 12, 2017
- Distribution pattern
- New York
- UPC, lot, and code information
- All lots (product is seasonal: September-November)
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Anderson's Frozen Custard
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.
