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FoodRecallWatch

Hi Tech Pharmaceuticals Recall History

4 Active Recalls

Hi Tech Pharmaceuticals has had 4 FDA-tracked food recalls since 2021, including 3 Class I recalls (most serious). 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
4
Years in FDA Data
Since 2021
Class I (Most Serious)
3
Most Common Reason
Undeclared allergens (3)
Latest Recall
May 12, 2021
First Recorded Recall
Apr 3, 2021
States Affected
48 states (nationwide)
Currently Active
4
Data Source
FDA openFDA + USDA FSIS
4
Total Recalls
3
Class I (Dangerous)
1
Class II
0
Class III

Complete Recall List (4 Records)

Every Hi Tech Pharmaceuticals recall in the FDA enforcement database, newest first. Each row links to the full recall notice with affected product codes, distribution, and consumer guidance.

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, Hi Tech Pharmaceuticals has 4 FDA food recalls on record, including 3 Class I (dangerous) recalls. There are currently 4 active recalls.

Hi Tech Pharmaceuticals currently has 4 active recalls. Check the recall details above to see if your specific product is affected. If you have a recalled product, do not consume it.

Hi Tech Pharmaceuticals's 4 recalls break down by severity: 3 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.

Hi Tech Pharmaceuticals recalls have affected 48 states (nationwide distribution). Check individual recall entries for specific distribution details.

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).

this entity is one of the data points covered by this site’s U.S. FDA food, drug, and device recalls dataset. The detail above comes directly from the FDA openFDA enforcement-report API; the context that follows situates the headline numbers against the broader distribution across U.S. consumer-product recalls.

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.