Samuel Adams Brewery CO Recall History
Samuel Adams Brewery CO has had 1 FDA-tracked food recall since 2015. 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
- 1
- Years in FDA Data
- Since 2015
- Class I (Most Serious)
- 0
- Most Common Reason
- N/A
- Latest Recall
- Jul 22, 2015
- First Recorded Recall
- Jul 22, 2015
- States Affected
- 22 states (nationwide)
- Currently Active
- 0
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (1 Records)
Every Samuel Adams Brewery CO 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 |
|---|---|---|---|
| Jul 22, 2015 | Apple Orchard Crisp Apple Hard Cider Three packages size... | 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, Samuel Adams Brewery CO has 1 FDA food recall on record, including 0 Class I (dangerous) recalls. There are no active recalls at this time.
Samuel Adams Brewery CO has no active recalls at this time. However, the brand has 1 historical recall. Always check this page for the latest recall status.
Samuel Adams Brewery CO's 1 recall break down by severity: 0 Class I (may cause serious health issues), 1 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.
Samuel Adams Brewery CO recalls have affected 22 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).
For this entity, the underlying data on this page comes from the FDA openFDA enforcement-report API. The breakdown above is the federal record; the paragraphs below add the per-entity context that makes the headline numbers usable for a real decision rather than just a data lookup.
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.