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Mel-O Cream Donuts International, Inc.

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

Mel-O Cream Donuts International, 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 Mel-O Cream Donuts International, Inc.

Date Product Reason Class
Oct 3, 2016 Jumbo Ring Donut; Best If Used By 02/26/2017; Approximate Unit Count: 84 Unit... Human fingertip found in product filling line. Class II
Oct 3, 2016 Hy Vee Long Johns (Red Raspberry Filled); Best If Used By 02/25/2017; Batch 1... Human fingertip found in product filling line. Class II
Oct 3, 2016 Jumbo Pershing (Cinnamon) Rolls; NET WT 11.25 and 16.1 Pounds; Approximate Un... Human fingertip found in product filling line. Class II
Oct 3, 2016 Hy Vee Shells (Bavarian Filled); Best If Used By 02/25/2017; Batch 162724703... Human fingertip found in product filling line. Class II
Oct 3, 2016 Arrowhead/Christmas Tree Shells; Best If Used By 02/26/2017; Batch 162734737;... Human fingertip found in product filling line. Class II
Oct 3, 2016 Hy Vee Long Shells (Red Raspberry Filled); Best If Used By 02/26/2017; Batch ... Human fingertip found in product filling line. Class II
Oct 3, 2016 Jumbo Apple Fritter; Approximate Unit Count: 6 Dozen; Mel-O-Cream Donuts Intl... Human fingertip found in product filling line. Class II
Oct 3, 2016 Fried Danish; Best If Used By 02/25/2017; Batch 162724711; NET WT 11.25 Pound... Human fingertip found in product filling line. Class II
Oct 3, 2016 Star Shaped Shells; Best If Used By 02/26/2017; Batch 162734736; NET WT 11.4... Human fingertip found in product filling line. Class II

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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