Summary
The FDA issued a Class II for Loard's Peppermint Ice Cream - 32 oz; 56 oz by Silver Moon LP dba Loard's Ice Cream. Reason: Undeclared Milk, Soy, Red #40..
Details
Source
Food Recall
External ID
H-0745-2026
Action Date
2026-05-13
Status
Ongoing
Category
food
Product Description
Loard's Peppermint Ice Cream - 32 oz; 56 oz
Lot/Code Info: None
Quantity Affected: 1061 units (32 oz/unit); 424 units (56 oz/unit)
Reason for Recall
Undeclared Milk, Soy, 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 II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
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 II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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-0745-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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