FDA recall,
Neogen Uniprim Powder for Horses
Neogen Uniprim Powder for Horses have a defective container closure.
Summary by Recall Canary from the FDA notice
What happened
Neogen Corporation is recalling Apple Flavored Uniprim Powder for Horses and Uniprim Powder for Horses due to a defective container closure. The products, manufactured by Neogen Corporation in Lexington, KY, were distributed nationwide within the U.S. The recall began on October 23, 2026, and was added to the FDA's Enforcement Report on October 24, 2026.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
2 products
Match the list below, then check the codes the FDA notice also names.
A UPC is the number printed under a barcode. An NDC (National Drug Code) is usually printed on the drug's label.
Apple Flavored UNIPRIM Powder for Horses, (trimethoprim and sulfadiazine), Net Contents: 400 grams
- NDC or UPC
- NDC 59051-3011-3
- UPC 7-26087-30021-4
- Lot code
- AUP1216251CC
- AUP1217251CC
- AUP0305261CC
- AUP0309261CC
- AUP0310261CC
- AUP0311261CC
- AUP0312261CC
- AUP0604261CC
- AUP0609261CC
- AUP0610261CC
- AUP0921261CC
- AUP0922261CC
- AUP0923261CC
- AUP0924261CC
UNIPRIM Powder for Horses, (trimethoprim and sulfadiazine), Net Contents: 400 grams
- NDC or UPC
- NDC 59051-3010-3
- UPC 7-26087-30017-7
- Lot code
- UP1211251CC
- UP1215251CC
- UP0526261CC
- UP0602261CC
From the FDA notice
UNIPRIM Powder for Horses, (trimethoprim and sulfadiazine), Net Contents: 400 grams, Manufactured by: Neogen Corporation, Lexington, KY 40511, NDC: 59051-3010-3, ANADA 200-033, UPC: 7-26087-30017-7
Recall details
- Company began the recall
- Sold in
Nationwide within the U.S.
- Company
- Neogen Corporation
- Hazard
- Packaging defect
- Event ID
- 100160
All recalls from Neogen Corporation
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
Listed on Recall Canary
