Silver Moon LP DBA Loard's Ice Cream Recall History
Silver Moon LP DBA Loard's Ice Cream has had 3 FDA-tracked food recalls since 2026. The full list below — sourced from the FDA openFDA enforcement database — shows dates, products, reasons, and classifications for every recall on record.
Key Facts
- Total Recalls
- 3
- Years in FDA Data
- Since 2026
- Class I (Most Serious)
- 0
- Most Common Reason
- Undeclared allergens (3)
- Latest Recall
- Apr 15, 2026
- First Recorded Recall
- Apr 15, 2026
- States Affected
- IN, CA
- Currently Active
- 3
- Data Source
- FDA openFDA + USDA FSIS
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Complete Recall List (3 Records)
Every Silver Moon LP DBA Loard's Ice Cream recall in the FDA enforcement database, newest first. Each row links to the full recall notice with affected product codes, distribution, and consumer guidance.
| Date | Product | Class | Status |
|---|---|---|---|
| Apr 15, 2026 | Banana Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehof... | Class II | Active |
| Apr 15, 2026 | Loard's Peppermint Ice Cream - 32 oz; 56 oz | Class II | Active |
| Apr 15, 2026 | Loard's Champagne Sherbert - 32 oz | Class II | Active |
Recall data sourced from the FDA's recalls and safety alerts database. Class I recalls indicate a reasonable probability of serious adverse health consequences. Always check the USDA FSIS recall list for meat and poultry products.
Frequently Asked Questions
Yes, Silver Moon LP DBA Loard's Ice Cream has 3 FDA food recalls on record, including 0 Class I (dangerous) recalls. There are currently 3 active recalls.
Silver Moon LP DBA Loard's Ice Cream currently has 3 active recalls. Check the recall details above to see if your specific product is affected. If you have a recalled product, do not consume it.
Silver Moon LP DBA Loard's Ice Cream's 3 recalls break down by severity: 0 Class I (may cause serious health issues), 3 Class II (may cause temporary health problems), and 0 Class III (unlikely to cause harm). See the full recall history table above for specific reasons.
Silver Moon LP DBA Loard's Ice Cream recalls have affected IN, CA. Check individual recall entries for specific distribution details.
Related
Recall data is sourced from the FDA openFDA enforcement database. Classifications reflect FDA severity ratings: Class I (dangerous), Class II (may cause temporary health problems), Class III (unlikely harmful).
this entity is one of the data points covered by this site’s U.S. FDA food, drug, and device recalls dataset. The detail above comes directly from the FDA openFDA enforcement-report API; the context that follows situates the headline numbers against the broader distribution across U.S. consumer-product recalls.
The methodology behind every numeric value on this page is publicly documented on the the FDA openFDA enforcement-report API portal and described in detail on this site’s methodology page. Refresh cadence varies by underlying series; the page surfaces the as-of date for each number so readers can trace any figure back to the source release.
For readers using this page as a decision input, the related-entity pages elsewhere on the site provide the comparison set. The most useful comparison for this entity is typically a peer within U.S. consumer-product recalls with similar size, similar exposure, or similar geography — not the national-level summary alone.