Peppermint Bon Bon Ice Cream (Cass Clay Creamery) – undeclared eggs (2012)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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
Brand
Cass Clay Creamery AMPI Fargo Division
Lot Codes / Batch Numbers
Brand code Hornbachers - 138M, 051M, Sunnybrook - 138M Schroeders - 060M
Products Sold
Brand code Hornbachers - 138M, 051M, Sunnybrook - 138M Schroeders - 060M
Cass Clay Creamery AMPI Fargo Division is recalling Peppermint Bon Bon Light Ice Cream under the following three brands: Hornbachers, Peppermint Bo due to The ice cream products may contain undeclared eggs. A flavoring containing egg yolks was used as an ingredient in the products, and the ingredient st. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IA, MN, ND, WI
Page updated: Jan 10, 2026