The Harvard Drug Group, LLC Recall History
The Harvard Drug Group, LLC has had 1 FDA-tracked food recall since 2014. 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 2014
- Class I (Most Serious)
- 0
- Most Common Reason
- Mislabeling (1)
- Latest Recall
- Dec 31, 2014
- First Recorded Recall
- Dec 31, 2014
- States Affected
- 27 states (nationwide)
- Currently Active
- 0
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (1 Records)
Every The Harvard Drug Group, LLC 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 |
|---|---|---|---|
| Dec 31, 2014 | Thera Tablets with Beta Carotene Dietary Supplement | 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, The Harvard Drug Group, LLC has 1 FDA food recall on record, including 0 Class I (dangerous) recalls. There are no active recalls at this time.
The Harvard Drug Group, LLC has no active recalls at this time. However, the brand has 1 historical recall. Always check this page for the latest recall status.
The Harvard Drug Group, LLC's 1 recall break down by severity: 0 Class I (may cause serious health issues), 0 Class II (may cause temporary health problems), and 1 Class III (unlikely to cause harm). See the full recall history table above for specific reasons.
The Harvard Drug Group, LLC recalls have affected 27 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.
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.