Pure Encapsulations, INC. Recall History
Pure Encapsulations, INC. has had 2 FDA-tracked food recalls since 2017. 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
- 2
- Years in FDA Data
- Since 2017
- Class I (Most Serious)
- 0
- Most Common Reason
- Undeclared allergens (2)
- Latest Recall
- Nov 17, 2017
- First Recorded Recall
- Nov 17, 2017
- States Affected
- AZ, CO, NH, NC, OH
- Currently Active
- 0
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (2 Records)
Every Pure Encapsulations, 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 |
|---|---|---|---|
| Nov 17, 2017 | Pure Encapsulations Systemic Enzyme Complex DIETARY SUPPL... | Class III | Terminated |
| Nov 17, 2017 | pure encapsulations AI Enzymes DIETARY SUPPLEMENT 120 CAP... | Class III | 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, Pure Encapsulations, INC. has 2 FDA food recalls on record, including 0 Class I (dangerous) recalls. There are no active recalls at this time.
Pure Encapsulations, INC. has no active recalls at this time. However, the brand has 2 historical recalls. Always check this page for the latest recall status.
Pure Encapsulations, INC.'s 2 recalls break down by severity: 0 Class I (may cause serious health issues), 0 Class II (may cause temporary health problems), and 2 Class III (unlikely to cause harm). See the full recall history table above for specific reasons.
Pure Encapsulations, INC. recalls have affected AZ, CO, NH, NC, OH. 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.
The methodology behind every numeric value on this page is publicly documented on the the FDA openFDA enforcement-report API portal and described in detail on this site’s methodology page. Refresh cadence varies by underlying series; the page surfaces the as-of date for each number so readers can trace any figure back to the source release.
For readers using this page as a decision input, the related-entity pages elsewhere on the site provide the comparison set. The most useful comparison for this entity is typically a peer within U.S. consumer-product recalls with similar size, similar exposure, or similar geography — not the national-level summary alone.