Loard's Maple Walnut Ice Cream Recall for Undeclared Allergens
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Silver Moon LP dba Loard's Ice Cream is recalling 405 units of Loard's Maple Walnut Ice Cream due to undeclared milk, walnuts, and sulfites.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on May 25, 2026 and geographically references Northern 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.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Food.
What Happened Silver Moon LP dba Loard's Ice Cream has initiated a voluntary recall of Loard's Maple Walnut Ice Cream because the product contains undeclared milk, walnuts, and sulfites.
Which Products Are Affected The recall involves Loard's Maple Walnut Ice Cream - 32 oz, with 405 units affected. The products were distributed to Loard's Ice Cream parlors and grocery stores in Northern California.
What You Should Do Consumers who have purchased the affected product should not consume it and should return it to the place of purchase or contact the recalling firm for further instructions.
Why This Matters Undeclared allergens pose a risk to individuals with sensitivities to milk, walnuts, or sulfites.
Source FDA Recall Number: H-0739-2026
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (771 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to May 25, 2026.
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