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Chris A Papas & Son Co

Complete recall history across all FDA and CPSC categories — 13 total recalls

Chris A Papas & Son Co 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 (13)

FDA food safety enforcement actions by Chris A Papas & Son Co

Date Product Reason Class
Jan 22, 2015 Pineapple During an FDA Investigation the firm was notified that their labels lack the ... Class II
Jan 22, 2015 Mint During an FDA Investigation the firm was notified that their labels lack the ... Class II
Jan 22, 2015 Vanilla During an FDA Investigation the firm was notified that their labels lack the ... Class II
Jan 22, 2015 Dark Opera Cream During an FDA Investigation the firm was notified that their labels lack the ... Class II
Jan 22, 2015 French Cream During an FDA Investigation the firm was notified that their labels lack the ... Class II
Jan 22, 2015 Cherry Easter Eggs During an FDA Investigation the firm was notified that their labels lack the ... Class II
Jan 22, 2015 Milk Chocolate Marshmallow Eggs During an FDA Investigation the firm was notified that their labels lack the ... Class II
Jan 22, 2015 Maple Nut During an FDA Investigation the firm was notified that their labels lack the ... Class II
Jan 22, 2015 Dark Chocolate Marshmallow Eggs During an FDA Investigation the firm was notified that their labels lack the ... Class II
Jan 22, 2015 Coconut Easter Eggs During an FDA Investigation the firm was notified that their labels lack the ... Class II
Jan 22, 2015 Peanut Butter During an FDA Investigation the firm was notified that their labels lack the ... Class II
Jan 22, 2015 White Opera Cream During an FDA Investigation the firm was notified that their labels lack the ... Class II
Jan 22, 2015 Milk Opera Cream During an FDA Investigation the firm was notified that their labels lack the ... 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.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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