Superior Fresh, LLC

Complete recall history across all FDA and CPSC categories, 6 total recalls

Superior Fresh, LLC 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 (6)

FDA food safety enforcement actions by Superior Fresh, LLC

Date Product Reason Class
Jan 10, 2023 Superior Fresh Organic Raw Spring Mix. 1 lb. Bag, 4 Count. UPC 8 57871-00827... Foreign material (small glass particles) Class II
Jan 10, 2023 Superior Fresh Mighty Mix, Net Wt. 4 oz. (113g). UPC 8 57871-00883 9. Ing... Foreign material (small glass particles) Class II
Jan 10, 2023 Superior Crunch Net Wt. 4 oz. (113g). Ingredients May Contain Green Leaf, G... Foreign material (small glass particles) Class II
Jan 10, 2023 Superior Fresh Organic Spring Mix Family Pack. UPC 8 50038-27430 6. Ingredi... Foreign material (small glass particles) Class II
Jan 10, 2023 Superior Fresh Lettuce Blend Ingredients May Contain Red Leaf, Green Leaf, G... Foreign material (small glass particles) Class II
Jan 10, 2023 Superior Fresh Lettuce Blend Ingredients May Contain Red Leaf, Green Leaf, G... Foreign material (small glass particles) 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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