Swire Coca Cola USA
Complete recall history across all FDA and CPSC categories, 3 total recalls
Swire Coca Cola USA 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 (3)
FDA food safety enforcement actions by Swire Coca Cola USA
| Date | Product | Reason | Class |
|---|---|---|---|
| Feb 19, 2022 | Coca-Cola Cherry Zero Sugar Fridge Pack, 12 - 12 FL OZ CANS (144 FL OZ) in a... | Exterior packaging correctly identifies the contents as Cherry Coca-Cola Zero... | Class II |
| Sep 12, 2018 | Caffeine-Free Barq s Root Beer 12 Pack, 12 oz cans | Recalling Caffeine-Free Barq s Root Beer 12 Pack due to mislabeling. | Class III |
| Mar 21, 2018 | Dr. Pepper Est. 1885 Diet, 20 FL Oz (1.25 PT), 591 mL | Swire Coca Cola is recalling certain Diet Dr Pepper bottle due to the potenti... | 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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