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Kraft Heinz Foods

Complete recall history across all FDA and CPSC categories — 9 total recalls

Kraft Heinz 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 (9)

FDA food safety enforcement actions by Kraft Heinz Foods

Date Product Reason Class
Dec 29, 2015 CapriSun tropical punch packaged in a blue and white box with pictures of fru... Possible presence of glass fragments in CapriSun and Kool-Aid Jammers. Class II
Dec 29, 2015 Kool-Aid Jammers Strawberry Kiwi packaged in a green and red box with white l... Possible presence of glass fragments in CapriSun and Kool-Aid Jammers. Class II
Dec 29, 2015 CapriSun fruit punch roarin'waters packaged in a blue and white box with pict... Possible presence of glass fragments in CapriSun and Kool-Aid Jammers. Class II
Dec 29, 2015 Kool-Aid Jammers Cherry packaged in a red box with white lettering. Possible presence of glass fragments in CapriSun and Kool-Aid Jammers. Class II
Dec 29, 2015 Kool-Aid Jammers Grape packaged in a purple and red box with white lettering. Possible presence of glass fragments in CapriSun and Kool-Aid Jammers. Class II
Dec 29, 2015 Kool-Aid Jammers Tropical Punch packaged in a red blue and purple box with wh... Possible presence of glass fragments in CapriSun and Kool-Aid Jammers. Class II
Jul 31, 2015 Kraft American Singles Pasteurized prepared cheese products packaged clear pl... The Kraft American Singles Pasteurized prepared cheese products contain a thi... Class II
Jul 31, 2015 Kraft American Singles white American Pasteurized prepared cheese products pa... The Kraft American Singles Pasteurized prepared cheese products contain a thi... Class II
Aug 29, 2014 Individually 2/3 oz. slices of American cheese product individually wrapped i... Kraft Foods Group is voluntarily recalling 7,691 cases of select varieties of... Class III

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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