Lakeside Foods, Inc

Complete recall history across all FDA and CPSC categories — 7 total recalls

Lakeside 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 (7)

FDA food safety enforcement actions by Lakeside Foods, Inc

Date Product Reason Class
Aug 10, 2017 IQF Green Beans, Keep Frozen. 11 varieties, packaged under the following bra... IQF French Style Green Beans and IQF Cut Green Beans may be contaminated with... Class II
Apr 3, 2017 Season's Choice Garden Fresh Sweet Peas, Net Wt 16 oz (1lb) 454g, Keep Frozen... The Season's Choice frozen peas, 16 oz., was tested and was positive for List... Class II
Feb 17, 2017 Kroger Peas & Carrots, Net Wt. 12 oz (340g), UPC 11110-89741; Harris Teete... Lakeside Foods is voluntarily recalling frozen green beans, peas and peas/ca... Class II
Feb 17, 2017 Kroger French Style Green Beans, Net Wt. 12 oz (340g), UPC 11110-89731 Lakeside Foods is voluntarily recalling frozen green beans, peas and peas/ca... Class II
Feb 17, 2017 Harris Teeter, Sweet Green Peas, 12 oz (340g), UPC 007203671652 Lakeside Foods is voluntarily recalling frozen green beans, peas and peas/ca... Class II
Nov 10, 2015 French Style Green Beans packaged under the following labels: 1. Giant Eagl... The 16 oz poly bags of IQF French Style Green Beans have the potential to be ... Class II
Aug 28, 2015 Frozen Peas & Carrots, Product is IQF, frozen, not ready to eat, each label c... The Ohio Department of Agriculture conducted testing on the product and found... 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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