Twin City Foods Inc

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

Twin City Foods 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 (6)

FDA food safety enforcement actions by Twin City Foods Inc

Date Product Reason Class
May 5, 2016 Central Markets Organics Green Peas, frozen, net wt. 16 oz. UPC 4122010240 ... Central Market Organic Peas recalled due to the potential for these products ... Class I
May 5, 2016 Central Markets Organics Mixed Vegetables, frozen, net wt. 16 oz. UPC 4122010... Organics Mixed Vegetables are recalled due to the potential for these product... Class I
Mar 20, 2015 Cadia Organic Cut Spinach, 16 oz. (454 g) frozen packages, UPC 15369 01165 Product has the potential to be contaminated with Listeria monocytogenes. Class II
Mar 20, 2015 Meijer Organics Chopped Spinach, 16 oz. (454 g) frozen packages, UPC 41250 02362 Product has the potential to be contaminated with Listeria monocytogenes. Class II
Mar 20, 2015 Wild Harvest Organic Cut Leaf Spinach, 16 oz. (454 g) frozen packages, UPC 11... Product has the potential to be contaminated with Listeria monocytogenes. Class II
Mar 20, 2015 Wegmans Organic Just Picked Spinach, 12 oz.(340g) frozen packages, UPC 77890 ... Product has the potential to be contaminated with Listeria monocytogenes. 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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