Class ITerminated in FDA datasetRecall initiated Jul 6, 2012

Peppermint Bon Bon Light Ice Cream under the following three brands: Hornbachers, Peppermint…

Recalling firm: Cass Clay Creamery AMPI Fargo Division

Why it was recalled

The ice cream products may contain undeclared eggs. A flavoring containing egg yolks was used as an ingredient in the products, and the ingredient statement on the product package…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Nov 27, 2012.

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ProductPeppermint Bon Bon Light Ice Cream under the following three brands: Hornbachers, Peppermint Bon Bon Light Ice Cream, Half Gallon (1.89 L), UPC 41130-21663, Distributed by Supervalu Inc, Eden Prairie, MN 55344. SunnyBrook, Peppermint Bon Bon Light Ice Cream, Half Gallon (1.89 L), UPC 70422-24919, Distributed by Mason Brothers Co., Wadena, MN 56482. Schroeder, Peppermint Bon Bon Ice cream, 56 oz or 1.75 Qt (1.65 L) 3 , UPC 72340-00193, Schroeder Company, Maplewood, MN 55113
Package size56 oz

FDA code information

Brand code Hornbachers - 138M, 051M, Sunnybrook - 138M Schroeders - 060M

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Full FDA record and distribution details

Original product description

Peppermint Bon Bon Light Ice Cream under the following three brands: Hornbachers, Peppermint Bon Bon Light Ice Cream, Half Gallon (1.89 L), UPC 41130-21663, Distributed by Supervalu Inc, Eden Prairie, MN 55344. SunnyBrook, Peppermint Bon Bon Light Ice Cream, Half Gallon (1.89 L), UPC 70422-24919, Distributed by Mason Brothers Co., Wadena, MN 56482. Schroeder, Peppermint Bon Bon Ice cream, 56 oz or 1.75 Qt (1.65 L) 3 , UPC 72340-00193, Schroeder Company, Maplewood, MN 55113

Original FDA recall reason

The ice cream products may contain undeclared eggs. A flavoring containing egg yolks was used as an ingredient in the products, and the ingredient statement on the product package did not reveal the presence of eggs.

Recall details

Recall number
F-1774-2012
Event ID
62513
FDA status
Terminated
Initiated
Jul 6, 2012
Reported
Aug 1, 2012
Classified
Jul 23, 2012
Terminated
Nov 27, 2012
Quantity
2492 units
Location
Fargo, ND, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

MN, WI, ND and IA

FDA source record · F-1774-2012

Data updated September 16, 2026. View official FDA data ↗

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