House Of Flavors, Inc.

Complete recall history across all FDA and CPSC categories — 9 total recalls

House Of Flavors, Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Food Recalls (9)

FDA food safety enforcement actions by House Of Flavors, Inc.

Date Product Reason Class
Feb 26, 2026 House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub Undeclared egg Class I
Feb 26, 2026 House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub Undeclared egg Not Yet Classified
Dec 12, 2025 2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8 Undeclared soy lecithin Class II
Dec 12, 2025 1972 Banana Pudding Ice Cream, 3 GAL, UPC 0 75196 00556 6 Undeclared soy lecithin Class II
Nov 11, 2024 Giant Eagle churned Butter Pecan Reduced Fat 48FLOZ, UPC 030034940430; 6 reta... Undeclared soy (soy lecithin). Class II
Nov 11, 2016 Ashby's Sterling Peanut Butter Landslide Ice Cream, 3 gallon container, frozen House of Flavors, Inc. is voluntarily recalling a limited portion of Ashby's... Class I
Jan 27, 2016 Purple Cow Limited Edition Cookie Butter Ice Cream, 8 oz. cups, packed in pap... House of Flavors, Inc. is voluntarily recalling a small batch of 8 oz. cups o... Class I
Dec 2, 2014 Dark Cocoa Sorbetto packed in 14 oz. plastic jars, 8 packages per case, manuf... Undeclared milk was found in 14 oz. Dark Cocoa Sorbetto gelato manufactured b... Class I
Mar 4, 2014 Belmont Premium Ice Cream, Chocolate Chip Cookie Dough, All Natural, 1.5 Qua... may contain undeclared nut allergen. Class I

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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