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FoodRecallWatch

Velvet Ice Cream Company Recall History

Velvet Ice Cream Company has had 11 FDA-tracked food recalls since 2012, including 11 Class I recalls (most serious). 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
11
Years in FDA Data
2012–2021
Class I (Most Serious)
11
Most Common Reason
Listeria contamination (10)
Latest Recall
Apr 23, 2021
First Recorded Recall
Oct 11, 2012
States Affected
IL, IN, KY, MI, NY, OH, PA, SC, VA, WV
Currently Active
0
Data Source
FDA openFDA + USDA FSIS
11
Total Recalls
11
Class I (Dangerous)
0
Class II
0
Class III

Complete Recall List (11 Records)

Every Velvet Ice Cream Company recall in the FDA enforcement database, newest first. Each row links to the full recall notice with affected product codes, distribution, and consumer guidance.

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, Velvet Ice Cream Company has 11 FDA food recalls on record, including 11 Class I (dangerous) recalls. There are no active recalls at this time.

Velvet Ice Cream Company has no active recalls at this time. However, the brand has 11 historical recalls. Always check this page for the latest recall status.

Velvet Ice Cream Company's 11 recalls break down by severity: 11 Class I (may cause serious health issues), 0 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.

Velvet Ice Cream Company recalls have affected IL, IN, KY, MI, NY, OH, PA, SC, VA, WV. Check individual recall entries for specific distribution details.

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).

The this entity record above pulls directly from the FDA openFDA enforcement-report API. What follows is the per-entity context — how this entity sits in the broader U.S. FDA food, drug, and device recalls distribution and which underlying factors drive the headline numbers.

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.

Practical use of this page is in combination with the comparison and ranking pages elsewhere on the site, which surface the same data for this entity’s peers within U.S. consumer-product recalls. A single-entity reading without peer context can be misleading when an entity is an outlier on one axis but typical on another.