Pepsico INC Recall History
Pepsico INC has had 3 FDA-tracked food recalls since 2019. The full list below — sourced from the FDA openFDA enforcement database — shows dates, products, reasons, and classifications for every recall on record.
Key Facts
- Total Recalls
- 3
- Years in FDA Data
- 2019–2023
- Class I (Most Serious)
- 0
- Most Common Reason
- Foreign material (2)
- Latest Recall
- Jan 28, 2023
- First Recorded Recall
- Aug 16, 2019
- States Affected
- 54 states (nationwide)
- Currently Active
- 0
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (3 Records)
Every Pepsico INC recall in the FDA enforcement database, newest first. Each row links to the full recall notice with affected product codes, distribution, and consumer guidance.
| Date | Product | Class | Status |
|---|---|---|---|
| Jan 28, 2023 | Starbucks frappuccino Vanilla. Chilled Coffee Drink. 13.... | Class II | Terminated |
| Aug 15, 2022 | Starbucks Vanilla Espresso Triple Shot, 15 oz, 12 bottles... | Class II | Terminated |
| Aug 16, 2019 | Diet Mountain Dew (Dewnited Michigan) 20 oz. plastic bo... | Class II | Terminated |
Recall data sourced from the FDA's recalls and safety alerts database. Class I recalls indicate a reasonable probability of serious adverse health consequences. Always check the USDA FSIS recall list for meat and poultry products.
Frequently Asked Questions
Yes, Pepsico INC has 3 FDA food recalls on record, including 0 Class I (dangerous) recalls. There are no active recalls at this time.
Pepsico INC has no active recalls at this time. However, the brand has 3 historical recalls. Always check this page for the latest recall status.
Pepsico INC's 3 recalls break down by severity: 0 Class I (may cause serious health issues), 3 Class II (may cause temporary health problems), and 0 Class III (unlikely to cause harm). See the full recall history table above for specific reasons.
Pepsico INC recalls have affected 54 states (nationwide distribution). Check individual recall entries for specific distribution details.
Related
Recall data is sourced from the FDA openFDA enforcement database. Classifications reflect FDA severity ratings: Class I (dangerous), Class II (may cause temporary health problems), Class III (unlikely harmful).
The this entity record above pulls directly from the FDA openFDA enforcement-report API. What follows is the per-entity context — how this entity sits in the broader U.S. FDA food, drug, and device recalls distribution and which underlying factors drive the headline numbers.
Every number on this page links back to the FDA openFDA enforcement-report API; the methodology page describes the inputs, refresh cadence, and known limitations of the underlying data product.
Practical use of this page is in combination with the comparison and ranking pages elsewhere on the site, which surface the same data for this entity’s peers within U.S. consumer-product recalls. A single-entity reading without peer context can be misleading when an entity is an outlier on one axis but typical on another.