Peppermint Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods) UPC: 8-12017-00933
Summary
The FDA issued a Class III for Peppermint Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, by Silver Moon LP dba Loard's Ice Cream. Reason: Undeclared Red #40.
Details
Source
Food Recall
External ID
H-0759-2026
Action Date
2026-05-13
Status
Ongoing
Category
food
Product Description
Peppermint Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods) UPC: 8-12017-00933
Lot/Code Info: UPC: 8-12017-00933
Quantity Affected: 1076 TOTAL units (32 oz/unit)
Reason for Recall
Undeclared Red #40
Distribution
Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-04-15
Company
San Leandro, CA
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 93 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Silver Moon LP dba Loard's Ice Cream has 48 FDA actions in our database, including 48 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Silver Moon LP dba Loard's Ice Cream) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Silver Moon LP dba Loard's Ice Cream have FDA actions?
Silver Moon LP dba Loard's Ice Cream has 48 FDA actions in our database, including 48 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0759-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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