FDA recall, , High risk
ADM Animal Nutrition MasterPlex 75P 30/30 RU
MasterPlex 75P medicated feed for cattle has incorrect labeling that can cause monensin or urea toxicity.
Recall ended May 14, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
ADM Animal Nutrition is recalling MasterPlex 75P 30/30 RU 55010CDH, MEDICATED, for Cattle Fed in Confinement for slaughter, because incorrect labeling resulted in monensin and/or urea toxicity in feed. The recall began January 12, 2026, and was added to the FDA's Enforcement Report on January 15, 2026.
The product, which contains monensin 700gm/ton, was distributed to Anson's Feed & Trucking in Atkinson, Nebraska. The recall involves 17,600 lbs of the feed.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for animal food:
- Keep the original packaging if you can: it shows the lot number, best-by or expiration date and UPC that identify the product.
- If you think your animal got sick or was hurt by it, you can report it to the FDA through the Safety Reporting Portal, with your veterinarian's contact information and diagnosis.
Is yours affected?
Compare the details below with your product and check the FDA notice to confirm whether it is affected.
Product details
ADM Animal Nutrition MasterPlex 75P 30/30 RU 55010CDH, MEDICATED, for Cattle Fed in Confinement for slaughter, ACTIVE DRUG INGREDIENTL Monensin 700gm/ton FEDING INSTRUCTIONS: Feed this product continuously at the rate of 0.75 lb per head per day by thoroughly mixing with a grain-roughage mixture to provide
- Strength
- 262.5 mg
- Lot code
- 218009
- 32925
Recall details
- Company began the recall
- Sold in
Anson's Feed & Trucking: 416 S. Sandy Lane Atkinson, Nebraska 68713
- Company
- ADM Animal Nutrition
- Hazard
- Chemical contamination
- Risk
High risk
There is a reasonable chance it could cause serious health problems or death in animals that eat it.
FDA Class I recall · How risk is rated
- Event ID
- 98293
- Recall number
- V-0061-2026
- Quantity recalled
- 17,600 lbs
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report
In FDA's weekly enforcement report
Classified by FDA
Listed on Recall Canary
Recall ended
Archived
