GloryBee Inc
Complete recall history across all FDA and CPSC categories — 4 total recalls
GloryBee 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 (4)
FDA food safety enforcement actions by GloryBee Inc
| Date | Product | Reason | Class |
|---|---|---|---|
| Jun 30, 2015 | Turkish Organic Diced Apricots with Rice Flour (5-7 mm), FOODIMPEX brand, Ite... | Product found to contain rocks and metal. | Class II |
| Jan 6, 2015 | Barley & Lentil Soup Spice Mix, sold under Aunt Patty's brand, packaged in 25... | Barley & Lentil Soup Spice Mix is recalled because it may contain traces of p... | Class I |
| Jan 6, 2015 | Mild Chili Powder, Salt-Free, sold under brand Aunt Patty's brand, packaged i... | Mild Chili Powder Salt Free is recalled because it contains more than 25 ppm ... | Class I |
| Jan 6, 2015 | Ground Cumin, sold under Aunt Patty's brand, packed in 1lb. pack, 5 lb. pack,... | Ground Cumin is recalled because it contains more than 25 ppm of peanut protein. | 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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