Brett Anthony Foods

Complete recall history across all FDA and CPSC categories, 5 total recalls

Brett Anthony Foods 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 (5)

FDA food safety enforcement actions by Brett Anthony Foods

Date Product Reason Class
Sep 13, 2018 Gotham Greens Classic Pesto 6.5 oz. plastic cup, 12 cups per case. Refriger... Ingredient declaration does not match principal display panel. Product is cl... Class II
Nov 9, 2015 Wild Mushroom Soup packaged in a 24 oz clear plastic container with green and... The Wild Mushroom soup was MIS-la bled and does not declare chestnuts. Class I
Nov 4, 2015 Tofu Curry Cous Cous Salad packaged in a clear plastic 16 oz box with a white... Undeclared Allergens. The Tofu Curry Cous Cous Box salad label does not decla... Class I
Aug 20, 2015 The product is in the form of a salad kit. It contains two plastic bags and o... Consumers found a piece of wire in Green Quinoa Cous Cous Salad. Class II
Jul 2, 2015 Vegetable Chili, 8 oz plastic container, labeled with a green and white label... The Vegetable Chili contains undeclared milk, an 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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