Imu-Tek Animal Health, Incorporated Recall History
Imu-Tek Animal Health, Incorporated has had 1 FDA-tracked food recall since 2025. 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 2025
- Class I (Most Serious)
- 0
- Most Common Reason
- Undeclared allergens (1)
- Latest Recall
- Nov 25, 2025
- First Recorded Recall
- Nov 25, 2025
- States Affected
- 16 states (nationwide)
- Currently Active
- 1
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (1 Records)
Every Imu-Tek Animal Health, Incorporated 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 25, 2025 | Imu-Tek Immuno-5 Colostrum Powder 7 oz. Intended Use: ... | Class II | Active |
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, Imu-Tek Animal Health, Incorporated has 1 FDA food recall on record, including 0 Class I (dangerous) recalls. There is currently 1 active recall.
Imu-Tek Animal Health, Incorporated currently has 1 active recall. Check the recall details above to see if your specific product is affected. If you have a recalled product, do not consume it.
Imu-Tek Animal Health, Incorporated'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.
Imu-Tek Animal Health, Incorporated recalls have affected 16 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.
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.