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FoodRecallWatch

Katies Korner INC. Recall History

Katies Korner INC. has had 1 FDA-tracked food recall since 2023. 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
1
Years in FDA Data
Since 2023
Class I (Most Serious)
0
Most Common Reason
Undeclared allergens (1)
Latest Recall
Sep 14, 2023
First Recorded Recall
Sep 14, 2023
States Affected
OH
Currently Active
0
Data Source
FDA openFDA + USDA FSIS
1
Total Recalls
0
Class I (Dangerous)
1
Class II
0
Class III

Complete Recall List (1 Records)

Every Katies Korner INC. recall in the FDA enforcement database, newest first. Each row links to the full recall notice with affected product codes, distribution, and consumer guidance.

DateProductClassStatus
Sep 14, 20233 Gallon, plastic container of mint chip flavored ice creamClass IITerminated

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, Katies Korner INC. has 1 FDA food recall on record, including 0 Class I (dangerous) recalls. There are no active recalls at this time.

Katies Korner INC. has no active recalls at this time. However, the brand has 1 historical recall. Always check this page for the latest recall status.

Katies Korner INC.'s 1 recall break down by severity: 0 Class I (may cause serious health issues), 1 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.

Katies Korner INC. recalls have affected OH. 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).

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.

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.