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Dollar Tree Distribution, Inc.

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

Recall Summary

4 Food Recalls 2 Drug Recalls 1 Device Recalls

Dollar Tree Distribution, Inc. appears in recall records across 3 categories. 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 (4)

FDA food safety enforcement actions by Dollar Tree Distribution, Inc.

Date Product Reason Class
Feb 18, 2022 Food products purchased from Family Dollar retail stores located in Alabama, ... Potential exposure to rodents and rodent activity in the distribution center. Class II
Feb 18, 2022 Dietary supplements purchased from Family Dollar retail stores located in Ala... Potential exposure to rodents and rodent activity in the distribution center. Class II
Dec 21, 2012 Candy Canes, Peppermint Flavor, 5 oz boxes, packed 12 individually candy cane... Candy product may contain metal and/or plastic pieces embedded in the candy. Class II
Dec 21, 2012 Candy Canes, Cherry Flavor, 5 oz boxes, packed 12 candy canes/box, and labele... Candy product may contain metal and/or plastic pieces embedded in the candy. Class II

Drug Recalls (2)

FDA drug safety enforcement actions by Dollar Tree Distribution, Inc.

Date Product Reason Class
Oct 5, 2023 Certain Over-The-Counter (OTC) drug products sold by Family Dollar retail sto... CGMP Deviations: OTC products were stored outside of labeled temperature requ... Class II
Feb 18, 2022 All Over-The-Counter (OTC) drug products sold by Family Dollar retail stores ... CGMP Deviations: Potential exposure to rodents and rodent activity in the dis... Class II

Device Recalls (1)

FDA medical device enforcement actions by Dollar Tree Distribution, Inc.

Date Product Reason Class
Feb 18, 2022 Medical Device products purchased from Family Dollar retail stores located in... Potential exposure to rodents and rodent activity in the distribution center. 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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