Loard's Lemon Chiffon Ice Cream Recall for Undeclared Allergens

Source: FDA · California

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Silver Moon LP dba Loard's Ice Cream is recalling 1,048 units of Loard's Lemon Chiffon Ice Cream due to undeclared milk, eggs, and Yellow #5.

What this FDA recall tells you, and what most readers miss

This notice was issued by FDA on May 24, 2026 and geographically references California. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.

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What Happened Silver Moon LP dba Loard's Ice Cream has initiated a voluntary recall of Loard's Lemon Chiffon Ice Cream because the product contains undeclared milk, eggs, and Yellow #5.

Which Products Are Affected The recall involves Loard's Lemon Chiffon Ice Cream in 32 oz units. A total of 1,048 units are affected. The recall number is H-0736-2026. Loard's brand products were distributed to Loard's Ice Cream parlors in Northern California, while private label products were distributed to grocery stores in Northern California.

What You Should Do Consumers should not consume the recalled product.

Why This Matters The recall affects products distributed across Northern California and involves undeclared allergens and color additive.

Source FDA recall H-0736-2026 (report date 20260513)

Original source: FDA Official Notice ↗

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Frequently Asked Questions

Common questions about this FDA recall.

What is this FDA recall about?
Silver Moon LP dba Loard's Ice Cream is recalling 1,048 units of Loard's Lemon Chiffon Ice Cream due to undeclared milk, eggs, and Yellow #5.
Which agency issued this alert?
This alert was issued by FDA. The original notice is available at the source link at the bottom of this article.
How severe is this alert?
This alert is classified as "medium" severity. Stay informed and follow agency guidance.
What area is affected?
This alert affects California. Check with FDA for the most current geographic scope.
Where can I find more FDA Recalls updates?
Browse the full FDA Recalls feed on Areazine at areazine.com/recalls/fda/ for the latest updates from FDA and other agencies.